HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862497Generated: October 30, 2026
Ethyl Acetate → (R)-1-(benzo[b]thiophen-5-yl)-2-bromoethanol
https://huagongshe.com/reaction/862497
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1-(1-Benzothiophen-5-yl)-2-bromo-1-ethanone | HCID 7060546 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-1-(benzo[b]thiophen-5-yl)-2-bromoethanol | HCID 53833740 | 94.3% |
Reaction Steps
A solution of 7.5 g of (+)-diisopinocamphenylchloroborane dissolved in 15 ml of tetrahydrofuran was cooled to -25° C. Thereto was added 4 g of 5-bromoacetylbenzo[b]thiophene. The resulting mixture was stirred for 4 hours at -20° C. to -15° C. The reaction mixture was added to a mixture of 80 ml of ethyl acetate and 80 ml of ice water. The organic layer was separated, washed with water and a saturated aqueous sodium chloride solution in this order, and dried over anhydrous magnesium sulfate. The solvent was removed by distillation under reduced pressure. The residue thus obtained was purified by column chromatography (eluant: hexane:ethyl acetate=10:1) to obtain 3.8 g of (R)-1-(benzo[b]thiophen-5-yl)-2-bromoethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05719150 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-094ed0bb374040ef8e5030eb962d269c |
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| Source note | uspto-grants-1998_02 |
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