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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 866782Generated: October 27, 2026

Sodium borohydride → HCID 20318590, compound

https://huagongshe.com/reaction/866782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant5-(N,N-dibenzylglycyl)-o-anisamideHCID 20318584—
SolventEthanolHCID 702—
ProductHCID 20318590HCID 2031859084.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04101579
Source datasetuspto-grants-1978_07
ORD IDord-0464a336d0c84de59eb1894c4ad7e640
Source noteuspto-grants-1978_07