GB364040A - Improvements in the manufacture of acidylated aromatic amines - Google Patents
Improvements in the manufacture of acidylated aromatic aminesInfo
- Publication number
- GB364040A GB364040A GB2897431A GB2897431A GB364040A GB 364040 A GB364040 A GB 364040A GB 2897431 A GB2897431 A GB 2897431A GB 2897431 A GB2897431 A GB 2897431A GB 364040 A GB364040 A GB 364040A
- Authority
- GB
- United Kingdom
- Prior art keywords
- spinning solution
- diacidyl
- benzidine
- finely
- purified
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 150000004982 aromatic amines Chemical class 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000009987 spinning Methods 0.000 abstract 4
- NOGFHTGYPKWWRX-UHFFFAOYSA-N 2,2,6,6-tetramethyloxan-4-one Chemical compound CC1(C)CC(=O)CC(C)(C)O1 NOGFHTGYPKWWRX-UHFFFAOYSA-N 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- HFACYLZERDEVSX-UHFFFAOYSA-N benzidine Chemical compound C1=CC(N)=CC=C1C1=CC=C(N)C=C1 HFACYLZERDEVSX-UHFFFAOYSA-N 0.000 abstract 2
- USIUVYZYUHIAEV-UHFFFAOYSA-N diphenyl ether Chemical compound C=1C=CC=CC=1OC1=CC=CC=C1 USIUVYZYUHIAEV-UHFFFAOYSA-N 0.000 abstract 2
- 239000000080 wetting agent Substances 0.000 abstract 2
- 150000008065 acid anhydrides Chemical class 0.000 abstract 1
- 125000003277 amino group Chemical group 0.000 abstract 1
- 150000004984 aromatic diamines Chemical class 0.000 abstract 1
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 abstract 1
- 238000009835 boiling Methods 0.000 abstract 1
- 229920002678 cellulose Polymers 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 239000006185 dispersion Substances 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 238000010348 incorporation Methods 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- GSPPYQYDYGNLGX-UHFFFAOYSA-N n-[4-(4-benzamidophenyl)phenyl]benzamide Chemical compound C=1C=CC=CC=1C(=O)NC(C=C1)=CC=C1C(C=C1)=CC=C1NC(=O)C1=CC=CC=C1 GSPPYQYDYGNLGX-UHFFFAOYSA-N 0.000 abstract 1
- 239000002245 particle Substances 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 239000000243 solution Substances 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 239000000725 suspension Substances 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Diacidyl aromatic diamines are obtained pure and in a fine state of subdivision suitable for incorporation in cellulose ester spinning solutions by treating a base containing two benzene residues linked directly as in benzidine or linked through an atom or group as in diphenylether and containing two amino groups with benzoic anhydride or other aromatic acid anhydride. In order to obtain the diacidyl compounds in a finely-divided state the acidylation is carried out in dilute solution, suspension, or dispersion, preferably at under boiling temperature with or without a wetting agent. The formed products may also be treated with wetting agents. They may be ground either wet or dry in order to reduce the particle size still further or they may be worked directly with the solvent to be used for the spinning solution or with the spinning solution itself for use as described in Specification 346,678. The starting materials may be purified as in Specification 363,986. In an example, purified benzidine is suspended in an excess of water, finely-ground benzoic anhydride is slowly added at 20-30 DEG C., and after further heating at 90 DEG C. the mixture is made alkaline and the dibenzoylbenzidine filtered, washed, treated with acetone and incorporated in the spinning solution. The Provisional Specification refers to the use of acid anhydrides in general.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2897431A GB364040A (en) | 1930-08-15 | 1930-08-15 | Improvements in the manufacture of acidylated aromatic amines |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2897431A GB364040A (en) | 1930-08-15 | 1930-08-15 | Improvements in the manufacture of acidylated aromatic amines |
Publications (1)
Publication Number | Publication Date |
---|---|
GB364040A true GB364040A (en) | 1931-12-15 |
Family
ID=10284206
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2897431A Expired GB364040A (en) | 1930-08-15 | 1930-08-15 | Improvements in the manufacture of acidylated aromatic amines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB364040A (en) |
-
1930
- 1930-08-15 GB GB2897431A patent/GB364040A/en not_active Expired
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