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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746624Generated: October 30, 2026

Benzyl Bromide → 2-(2-Benzyloxy-ethyl)-3-bromo-benzo[b]thiophene

https://huagongshe.com/reaction/746624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
ReactantHCID 821949HCID 821949—
SolventDimethylformamideHCID 6228—
Product2-(2-Benzyloxy-ethyl)-3-bromo-benzo[b]thiopheneHCID 5859155887.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a cooled solution (0° C.) of 2-(3-bromo-benzo[b]thiophen-2-yl)-ethanol (7.7 g, 29.9 mmol) in DMF (40 mL), NaH (1.44 g, 59.8 mmol, 95%) was added and the mixture was stirred for 20 min at 0° C. Subsequently benzylbromide (5.3 mL, 45 mmol) was added and the mixture was stirred overnight while the temperature gradually reached room temperature. After quenching with MeOH, the mixture was concentrated in vacuo, dissolved in EtOAc, washed with sat NaHCO3, brine, dried (Na2SO4) and concentrated in vacuo. Purification by silica gel column chromatography (eluent: EtOAc/Hexanes=1/1) afforded 9.1 g of 2-(2-benzyloxy-ethyl)-3-bromo-benzo[b]thiophene (87% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07393865B2
Source datasetuspto-grants-2008_07
ORD IDord-c671ffe1551b4822ac34247c47b82dc2
Source noteuspto-grants-2008_07