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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1787336Generated: October 31, 2026

Sodium borohydride → HCID 23114129, compound

https://huagongshe.com/reaction/1787336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23114301HCID 23114301—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 23114129HCID 2311412916%

Reaction Steps

To a solution of N-(7-acetyl-3-(4-isopropylphenyl)-4,6-dimethyl-2,3-dihydro-1-benzofuran-5-yl)-N′-(tert-butyl)urea (718 mg, 1.7 mmol) obtained in Example 204 in methanol (10 mL) was added sodium borohydride (64.3 mg, 1.7 mmol) at 0° C., and the resulting mixture was stirred for 3 hours. The reaction solution was diluted with water and the product was extracted with ethyl acetate. The extract was washed with saturated brine, dried over sodium sulfate, and then concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane:ethyl acetate=1:1) to obtain 115 mg (yield: 16%) of the title compound having high polarity of two isomers. Melting point: 212-214° C. (ethyl acetate-hexane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507841B2
Source datasetuspto-grants-2009_03
ORD IDord-d07e7d4a88b14e7ebe3265d9df62d5b4
Source noteuspto-grants-2009_03