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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591438Generated: October 26, 2026

Acetic Acid → Methyl 2-[6-hydroxy-4-(trifluoromethyl)benzo[b]thiophen-3-yl]acetate

https://huagongshe.com/reaction/591438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrogen BromideHCID 260—
ReactantMethyl 2-[6-methoxy-4-(trifluoromethyl)benzo[b]thiophen-3-yl]acetateHCID 121004362—
SolventSodium chloride; waterHCID 57417360—
ProductMethyl 2-[6-hydroxy-4-(trifluoromethyl)benzo[b]thiophen-3-yl]acetateHCID 89767967—

Reaction Conditions

Temperature130 °C

Reaction Steps

To a mixture of methyl(6-methoxy-4-(trifluoromethyl)-1-benzothiophen-3-yl)acetate obtained above (405 mg) and AcOH (1.5 mL) was added 48% hydrobromic acid (3 mL) at room temperature. The mixture was stirred at 130° C. for 40 min under microwave irradiation. The mixture was poured into brine at room temperature and extracted with EtOAc. The organic layer was separated, washed with brine, dried over MgSO4 and concentrated in vacuo. A mixture of the residue, MeOH and conc. H2SO4 (0.071 mL) was refluxed for 1 h. The mixture was poured into brine at room temperature and extracted with EtOAc. The organic layer was separated, washed with brine twice, dried over MgSO4 and concentrated in vacuo. The residue was purified by silica gel column chromatography (EtOAc/hexane) to give the title compound (232 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09238639B2
Source datasetuspto-grants-2016_01
ORD IDord-03b42150b72e46f9888fe788df691f56
Source noteuspto-grants-2016_01