Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 732818Generated: October 30, 2026

Water → 6-(Benzyloxy)-2,3-dibromo-1-benzothiophene

https://huagongshe.com/reaction/732818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzyl BromideHCID 7498—
ReactantSodium hydrideHCID 24758—
Reactant2,3-Dibromo-benzo[b]thiophen-6-olHCID 69072160—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product6-(Benzyloxy)-2,3-dibromo-1-benzothiopheneHCID 6907524992%

Reaction Steps

Add a solution of 2,3-dibromo-benzo[b]thiophen-6-ol (43.9 g, 143 mmol) in DMF (1000 mL), dropwise, to a suspension of sodium hydride in DMF (1.5 L) at 0° C. Stir for 20 minutes, add benzyl bromide (17 mL, 143 mmol). Remove ice bath, and stir at room temperature for 2 hours. Pour reaction mixture into water (8 L) and ethyl acetate (4 L) and stir overnight. Separate layers and wash organic layer with water (3×800 mL) and brine (800 mL). Dry with sodium sulfate, filter, and concentrate in vacuo to give 52.4 g of 6-benzyloxy-2,3-dibromo-benzo[b]thiophene (92%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07585977B2
Source datasetuspto-grants-2009_09
ORD IDord-a1f7a1a496b846c1bc39cc77fa09d9b3
Source noteuspto-grants-2009_09