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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553214Generated: October 26, 2026

Sulfuric Acid → 2-(1-Benzothiophen-5-yl)ethan-1-ol

https://huagongshe.com/reaction/553214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium borohydrideHCID 4311764—
ReactantBenzo[b]thiophene-5-acetic acidHCID 11469582—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product2-(1-Benzothiophen-5-yl)ethan-1-olHCID 1198337185.6%

Reaction Steps

To 340 mL of tetrahydrofuran was suspended 50.2 g of sodium borohydride, to which were dropped tetrahydrofuran (340 mL) solution of 170 g of (1-benzothiophen-5-yl)acetic acid, and 65.1 g of sulfuric acid successively, which was then stirred at room temperature for 2.5 hours. To this reaction mixture was dropwise added 85 mL of acetone, which was then stirred for 30 minutes. Thereto were added 510 mL of water and 680 mL of toluene. The organic layer was separated, to which was added 510 mL of water, and the pH was adjusted to 12 with 48 mL of 20% (w/w) sodium hydroxide aqueous solution. The organic layer was separated, and washed with water, followed by distilling off the solvent. Thereto were added cyclohexane and toluene. The precipitate was collected by filtration to provide 135 g of 2-(1-benzothiophen-5-yl)ethanol as white solid form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07951963B2
Source datasetuspto-grants-2011_05
ORD IDord-e293466984bb4d4184938ef19f57e46b
Source noteuspto-grants-2011_05