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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390970Generated: October 29, 2026

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

https://huagongshe.com/reaction/2390970

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 numberUS08273902B2
Source datasetuspto-grants-2012_09
ORD IDord-86f68d1aa9ad4e04b4be03c0f716db64
Source noteuspto-grants-2012_09