HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 13293071, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 13435388 | HCID 13435388 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13293071 | HCID 13293071 | 35% |
Reaction Steps
To a stirred solution of 2-acetamido-7-methoxy-3,4-dihydronaphthalen 1(2H)-one in absolute ethanol (100 ml) was added sodium borohydride (1.6 gms, 0.04 m) in portions. After stirring for 1/2 hour, acetic acid was added to decompose any excess sodium borohydride. The reaction mixture was poured onto water (150 ml) and this was extracted with ethyl acetate (3×150). The ethyl acetate was washed with aqueous saturated sodium chloride, and was dried over anhydrous sodium sulfate. After filtration, the ethyl acetate was removed under reduced pressure (20 mm) to give a semisolid. The solid was slurried with ether and filtered to yield 3.3 gms (35%) of product as a white solid, m.p. 135°-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04420480 |
| Source dataset | uspto-grants-1983_12 |
| ORD ID | ord-505e05079b074c3fb210d1b77d465fab |
| Source note | uspto-grants-1983_12 |