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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 590964Generated: October 29, 2026

Water → Methyl 2-(2-bromo-1-benzothiophen-3-yl)-2-(tert-butoxy)acetate

https://huagongshe.com/reaction/590964

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-(1-benzothiophen-3-yl)-2-(tert-butoxy)acetateHCID 70813710—
SolventAcetonitrileHCID 6342—
ProductMethyl 2-(2-bromo-1-benzothiophen-3-yl)-2-(tert-butoxy)acetateHCID 7081372945%

Reaction Steps

N-bromosuccinimide (67 mg, 0.37 mmol) was added at room temperature to a stirred solution of methyl 2-(1-benzothiophen-3-yl)-2-(tert-butoxy)acetate (4b) (70 mg, 0.25 mmol) in acetonitrile (2 mL) under a nitrogen atmosphere. After 20 hours, water (10 mL) was added and the reaction mixture was extracted with dichloromethane (2×10 mL). The organic layer was washed with brine (10 mL), dried over sodium sulfate, filtered and evaporated to dryness. The residue was purified by flash chromatography on silica gel (cyclohexane/ethyl acetate 90/10) to afford the desired product (4c) as a pale oil (40 mg, 0.11 mmol, 45%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238026B2
Source datasetuspto-grants-2016_01
ORD IDord-44f5cbeafb6b4fdc9a1c743a8fb6ef00
Source noteuspto-grants-2016_01