HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375519Generated: October 29, 2026
Acetic Anhydride → HCID 18993030, compound
https://huagongshe.com/reaction/375519
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 2-(4-Chlorophenyl)ethylamine | HCID 67430 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | 2-AMINO-4-METHYL-3-FURONITRILE | HCID 11018853 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 18993030 | HCID 18993030 | — |
Reaction Steps
A mixture of 4.0 g of 2-amino-3-cyano-4-methylfuran, 3 cc of triethylorthoformate, and 0.05 cc of acetic anhydride was heated to 135° C. for three hours. Then 5 g of 2-(4-chlorophenyl)ethylamine, 5 cc of glacial acetic acid, and 3.2 g of sodium acetate were added to the reaction mixture. The temperature of the mixture was maintained at 135° C. for three additional hours, after which the mixture was cooled, treated with water and extracted with dichloromethane. The organic phase was then concentrated and washed with water. The solids were extracted from the organic phase with large volumes of ether, which were combined and concentrated to provide 1.07 g of product. M. P. 140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05486516 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-f43d2e5d48eb4f919148ad48efc34c84 |
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| Source note | uspto-grants-1996_01 |
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