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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 553215Generated: November 1, 2026

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

https://huagongshe.com/reaction/553215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
ReactantSodium borohydrideHCID 4311764—
ReactantBenzo[b]thiophene-5-acetic acidHCID 11469582—
ReactantHydrochloride 1,2-dimethoxyethaneHCID 86628724—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Solvent1,2-DimethoxyethaneHCID 8071—
Product2-(1-Benzothiophen-5-yl)ethan-1-olHCID 1198337184.6%

Reaction Steps

To 5 mL of 1,2-dimethoxyethane was suspended 2.95 g of sodium borohydride, to which were dropwise added 1,2-dimethoxyethane (25 mL) solution of 10 g of (1-benzothiophen-5-yl)acetic acid, and 11 mL of 6.9 mol/L hydrochloride/1,2-dimethoxyethane solution, which was then stirred at room temperature for 1 hour. To this reaction mixture was dropwise added 5 mL of acetone, which was then stirred for 30 minutes. Thereto were added 20 mL of water, 30 mL of toluene and 2 mL of 2 mol/L hydrochloric acid. Next, after the pH was adjusted to 9.5 with 20 mL of 2 mol/L sodium hydroxide aqueous solution, the organic layer was separated. The organic layer was dried over anhydrous magnesium sulfate, followed by distilling off the solvent. Thereto were added cyclohexane and toluene. The precipitate was collected by filtration to provide 7.84 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-e9b2e82a5c4d440282131279363fa2c8
Source noteuspto-grants-2011_05