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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403314Generated: November 4, 2026

Sodium borohydride → HCID 86671405, compound

https://huagongshe.com/reaction/2403314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantSodium MethoxideHCID 10942334—
Reactant1261859-54-4HCID 53350327—
Reactant2-Bromo-1-(4-bromo-3-chlorophenyl)ethan-1-oneHCID 58302329—
SolventEthanolHCID 702—
Solventtert-Butyl methyl etherHCID 15413—
ProductHCID 86671405HCID 86671405—

Reaction Steps

To a stirred solution of the mixture of 2-bromo-1-(4-bromo-3-chlorophenyl)ethanone and 2-chloro-1-(4-bromo-3-chlorophenyl)ethanone (18.4 g) in ethanol (200 ml) at 5° C. was added portionwise over 5 min NaBH4 (2.23 g). The reaction mixture was then stirred at room temperature for 90 min to afford a yellow solution. TLC analysis showed the reaction was complete. Sodium methoxide (1.59 g) was then added and the reaction mixture was stirred at 50° C. for 4 h. TLC analysis showed the reaction was complete. The reaction mixture was then poured into TBME and washed with saturated brine. The organic layer was separated, then dried over Na2SO4 and concentrated in vacuo to afford (RS)-2-(4-bromo-3-chloro-phenyl)-oxirane (15.2 g) as a brown oil which was used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802673B2
Source datasetuspto-grants-2014_08
ORD IDord-8d3a2d8143614f579a8c787d76ffc837
Source noteuspto-grants-2014_08