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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234790Generated: October 25, 2026

LY88074 Trimethyl ether → 2-(4-Methoxyphenyl)-3-(4-Hydroxybenzoyl)-6-Methoxybenzo[b]thiophene

https://huagongshe.com/reaction/234790

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLY88074 Trimethyl etherHCID 9953060—
ReactantHCID 45051917HCID 45051917—
SolventHydrochloric AcidHCID 313—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2-(4-Methoxyphenyl)-3-(4-Hydroxybenzoyl)-6-Methoxybenzo[b]thiopheneHCID 9865197—

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 0.4 g (1 mmol) of [6-Methoxy-2-(4-methoxyphenyl)benzo[b]thien-3-yl][4-methoxyphenyl]methanone in 2 mL of DMF was added to a solution of 3 mL of 0.5M sodium ethanethiol in DMF. The reaction mixture was heated to 80° C. for 4 hours. The reaction mixture was allowed to cool and diluted with 10 mL of water and 10 mL of EtOAc and neutralized with 1N HCl. The reaction mixture was extracted three times with 30 mL portions of EtOAc. The combined organic extracts were washed four times with 20 mL portions of brine and dried with MgSO4 and evaporated to dryness. The crude product was chromatographed on silica eluting with 30% EtOAc in hexane, and evaporated to dryness. This yielded 0.31 g of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05596106
Source datasetuspto-grants-1997_01
ORD IDord-7df6a894b87446858f7b70e9573da166
Source noteuspto-grants-1997_01