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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1851338Generated: November 2, 2026

3-Chlorothiophene → 2-Acetyl-3-chlorothiophene

https://huagongshe.com/reaction/1851338

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-ChlorothiopheneHCID 87017—
ReactantN-Methoxy-N-methylacetamideHCID 537505—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventSodium chloride; waterHCID 57417360—
Product2-Acetyl-3-chlorothiopheneHCID 1487253104.6%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of 3-chlorothiophene (4.80 g, 40.48 mmol) in THF (50 mL) was added BuLi (2.5N in hexane, 17.9 mL) at −30° C. After addition, the mixture was stirred for 30 min at −10° C., and then cooled to −45° C. N-methoxy-N-methyl acetamide (55.0 g, 48.8 mmol) was added and allowed to warm to room temperature during 40 min and maintained for an additional 20 min. Brine (80 mL) was added to quench the reaction, extracted with EA (60 mL×3). The combined organic layers were dried over anhydrous Na2SO4, filtered, concentrated to afford 24-1 (˜80% pure) as a yellow oil (6.80 g) which used for the next step directly.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957105B2
Source datasetuspto-grants-2015_02
ORD IDord-c27b3537808b45a7ad5c6724b7fe743d
Source noteuspto-grants-2015_02