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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546255Generated: October 26, 2026

Water → 2,3-Dihydrobenzo(b)thiophene

https://huagongshe.com/reaction/546255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,3-Dihydro-1lambda6-benzothiophene-1,1-dioneHCID 284423—
ReactantAluminium lithium hydrideHCID 21226445—
SolventHydrochloric AcidHCID 313—
SolventDiethyl EtherHCID 3283—
Product2,3-Dihydrobenzo(b)thiopheneHCID 7831946%

Reaction Conditions

Temperature0 °C

Reaction Steps

A suspension of 2,3-dihydro-benzo[b]thiophene 1,1-dioxide (5.06 g, 30.08 mmol) in diethyl ether (150 mL) was added to a suspension of lithium aluminum hydride (10.27 g, 270.27 mmol) in diethyl ether (150 mL) at 25° C. After this time it was heated to reflux for 4 h (caution: if heating is too rapid it can exotherm rapidly and cause loss of material through the reflux condenser). It was then cooled to 0° C. in an ice bath and water (50 mL) was added very slowly. The resulting material was dissolved in 4 M aqueous hydrochloric acid (1 L). The aqueous layer was then extracted with diethyl ether (3×200 mL). The organic layers were combined and dried over magnesium sulfate, filtered and concentrated in vacuo. The material was purified by passing it through a plug of silica gel using pentane as the solvent to afford 2,3-dihydro-benzo[b]thiophene (1.88 g, 46%) as a clear colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935699B2
Source datasetuspto-grants-2011_05
ORD IDord-11fb6e12e91a4bf2bad0804052390e4c
Source noteuspto-grants-2011_05