HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116678Generated: October 27, 2026
Acetic Anhydride → (E)-2-acetylamino-3-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-acrylic acid
https://huagongshe.com/reaction/2116678
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Acetylglycine | HCID 10972 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 4-Amino-3-chloro-5-(trifluoromethyl)benzaldehyde | HCID 13020473 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (E)-2-acetylamino-3-(4-amino-3-chloro-5-trifluoromethyl-phenyl)-acrylic acid | HCID 66941463 | — |
Reaction Steps
A mixture of 50.0 g (224 mmol) 4-amino-3-chloro-5-trifluoromethyl-benzaldehyde, 39.3 g (335 mmol) N-acetylglycine, 27.5 g (335 mmol) sodium acetate and 200 ml acetic anhydride was stirred for 2 hours in an oil bath at an oil bath temperature of 128° C. After cooling to an oil bath temperature of 90° C. 100 ml of water were added dropwise and the resulting suspension was added to a mixture of 1000 ml of water and 500 ml of toluene. The precipitate formed was suction filtered, washed with 300 ml of toluene and 500 ml of water and dried overnight at 60° C. in the circulating air dryer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07439237B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-10dfa442898848b5a73b028f43127b1b |
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| Source note | uspto-grants-2008_10 |
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