HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 20318590, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 5-(N,N-dibenzylglycyl)-o-anisamide | HCID 20318584 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 20318590 | HCID 20318590 | 84.9% |
Reaction Steps
A solution of 5-(N,N-dibenzylglycyl)-o-anisamide (13.0g) in ethanol (800ml) was treated with excess solid sodium borohydride (ca.2g) and allowed to stand overnight at room temperature. The ethanol was then evaporated under reduced pressure and the residue partitioned between ethyl acetate and water. The ethyl acetate was separated, washed with brine, dried over MgSO4 and evaporated. The residue readily crystallised on trituration with ether to afford 5-(2-dibenzylamino-1-hydroxyethyl)-o-anisamide as a white solid (11.1g) m.p. 120°-123°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04101579 |
| Source dataset | uspto-grants-1978_07 |
| ORD ID | ord-0464a336d0c84de59eb1894c4ad7e640 |
| Source note | uspto-grants-1978_07 |