HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403314Generated: November 4, 2026
Sodium borohydride → HCID 86671405, compound
https://huagongshe.com/reaction/2403314
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1261859-54-4 | HCID 53350327 | — |
| Reactant | 2-Bromo-1-(4-bromo-3-chlorophenyl)ethan-1-one | HCID 58302329 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | HCID 86671405 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802673B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-8d3a2d8143614f579a8c787d76ffc837 |
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| Source note | uspto-grants-2014_08 |
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