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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553216Generated: October 31, 2026

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

https://huagongshe.com/reaction/553216

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantSodium borohydrideHCID 4311764—
ReactantBenzo[b]thiophene-5-acetic acidHCID 11469582—
SolventTetrahydrofuranHCID 8028—
Product2-(1-Benzothiophen-5-yl)ethan-1-olHCID 1198337189%

Reaction Conditions

Temperature66 °C

Reaction Steps

To 40 mL of tetrahydrofuran was suspended 4.72 g of sodium borohydride, to this solution were dropwise added tetrahydrofuran (60 mL) solution of 20 g of (1-benzothiophen-5-yl)acetic acid, and 6.12 g of sulfuric acid. The solution was heated to 66° C., followed by distilling off about 40 mL of the solvent under normal pressure, which was then stirred at same temperature for 1 hour. After cooling, to this reaction mixture was dropwise added 10 mL of acetone, which was then stirred for 30 minutes. Thereto were added 90 mL of water and 80 mL of toluene. The organic layer was separated, to which was added 60 mL of water, and the pH was adjusted to 13.6 with 5 mL of 5 mol/L sodium hydroxide aqueous solution. The organic layer was separated, washed with water, followed by distilling off the solvent, and thereto were added cyclohexane and toluene. The precipitate was collected by filtration to provide 16.5 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-d8fa05fef4104be883c6676eaba4a101
Source noteuspto-grants-2011_05