HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 12925977, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | alpha-[(5-Acetylamino-4-chloro-2-methoxycarbonylphenyl)oxy]-gamma-butyrolactone | HCID 12925954 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 12925977 | HCID 12925977 | — |
Reaction Steps
A mixture of 23 g. of α-[(5-acetylamino-4-chloro-2-methoxycarbonylphenyl)oxy]-γ-butyrolactone, 46 ml. of triethylamine and 230 ml. of acetic anhydride was heated at 120° C. for 5 hours. The solvents were evaporated off under reduced pressure, then the residue was poured into ice-water. The precipitating crystals were collected by filtration, washed with water and dried, followed by recrystallization from ethyl acetate to give 6-diacetylamino-5-chloro-4',5'-dihydrospiro[benzo[b]furan-2(3H), 3'(2'H)-furan]-2',3-dione melting at 181°-185° C. Yield 6.8 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04284644 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-5a18b612b4f74cafa6646bbe3476d4dc |
| Source note | uspto-grants-1981_08 |