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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387044Generated: November 1, 2026

Methanesulfonic Acid → 2-Dimethylamino-5-fluoro-6-methoxybenzo[b]thiophene

https://huagongshe.com/reaction/1387044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonic AcidHCID 6395—
ReactantN,N-dimethyl-3-fluoro-4-methoxy-2-hydroxyphenylthioacetamideHCID 21182765—
SolventDichloromethaneHCID 6344—
Product2-Dimethylamino-5-fluoro-6-methoxybenzo[b]thiopheneHCID 10775569139.3%

Reaction Steps

A solution of 16.6 g (68.2 mmol) of N,N-dimethyl-3-fluoro-4-methoxy-2-hydroxyphenylthioacetamide (Part A) in 400 mL of CH2Cl2 was treated with 22.0 mL (339.0 mmol) of MeSO3H in a dropwise manner. The reaction was stirred at room temperature for 4 h, was cooled to 0° C., and was quenched by the careful addition of 500 mL of saturated aqueous NaHCO3. The two layers were separated and the aqueous layer was extracted with EtOAc (5×200 mL). The combined organic layers were washed with 500 mL of saturated aqueous NaHCO3 and 500 mL of H2O, dried over Na2SO4, and filitered. Evaporation of the solvent in vacuo afforded 21.4 g of an oil which was purified by flash chormatography (SiO2; gradient of 10% then 20% EtOAc in hexanes) to give 2.87 g (12.7 mmol; 19%) of the title compound as a light pink solid

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265575B1
Source datasetuspto-grants-2001_07
ORD IDord-ddf33b6878fa43b3ba7bc1698d873b2f
Source noteuspto-grants-2001_07