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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492645Generated: October 30, 2026

Sodium borohydride → HCID 19934850, compound

https://huagongshe.com/reaction/1492645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantMethyl 2-(2,6-dimethyl-4-formylphenoxy)-2-(3-chlorophenyl)acetateHCID 18950590—
SolventMethanolHCID 887—
ProductHCID 19934850HCID 1993485063%

Reaction Steps

To a solution of 1.260 g (3.79 mmol) of the product of Step A in 8 mL methanol was added 0.072 g (1.90 mmol) of sodium borohydride and the reaction mixture was stirred at room temperature for 15 minutes. Excess borohydride was quenched with water, and the reaction mixture was extracted into EtOAc. The organic layer was dried (MgSO4), filtered, evaporated, and then purified on a silica gel flash chromatography column eluted with 30% EtOAc-hexane. The purified fractions were combined, evaporated and dried in vacuo to afford 0.790 g (63%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05374638
Source datasetuspto-grants-1994_12
ORD IDord-c3747f79d2f642da9692d4d8e3c71bda
Source noteuspto-grants-1994_12