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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1069629Generated: October 31, 2026

Sodium borohydride → HCID 10735747, compound

https://huagongshe.com/reaction/1069629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 10830680HCID 10830680—
SolventEthanolHCID 702—
ProductHCID 10735747HCID 1073574788%

Reaction Steps

A mixture of 1 g (3 mmol) of 2-ethyl-4-methoxy-alpha-oxo-1-(phenylmethyl)-1H-indole-3-acetamide and 142 mg (3.75 mmol) of sodium borohydride and 100 mL of ethanol was stirred for 20 hours, and evaporated at reduced pressure. The residue was taken up in ethyl acetate and water, the ethyl acetate separated and washed with brine and dried (MgSO4). The solution was concentrated at reduced pressure and the residue stirred with ether. The insoluble material was filtered to give 893 mg (88%) of 2-ethyl-4-methoxy-alpha-hydroxy-1-(phenylmethyl)-1H-indole-3-acetamide, mp, 160-162° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06252084B1
Source datasetuspto-grants-2001_06
ORD IDord-ab4c4e407f9f4729a436ec68d3a8b271
Source noteuspto-grants-2001_06