HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 12908984, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 6-(2,4-Difluorophenoxy)-2,3-dihydro-1H-inden-5-amine | HCID 12887086 | — |
| Catalyst | chromium (VI) trioxide | HCID 10219390 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12908984 | HCID 12908984 | — |
| Product | HCID 12908985 | HCID 12908985 | — |
Reaction Steps
13.9 g of 6-(2,4-difluorophenoxy)-5-indanylamine in 93 ml of acetic acid was combined at 30° C. with 40 ml of acetic anhydride. Thereafter a solution of 11 g of chromium trioxide in 27 ml of water and 17 ml of acetic acid was added dropwise at 50° C. After another 40 minutes at 50° C., the mixture was cooled, poured on ice water, and vacuum-filtered. The residue was chromatographed over silica gel with dichloromethane-ethyl acetate, thus obtaining 9 g of 5-acetylamino-6-(2,4-difluorophenoxy)-1-indanone, mp 153° C., and subsequently 4 g of the isomeric 6-acetylamino-5-(2,4-difluorophenoxy)-1-indanone, mp 199° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04375479 |
| Source dataset | uspto-grants-1983_03 |
| ORD ID | ord-534865baf2334f04bf72389d58730326 |
| Source note | uspto-grants-1983_03 |