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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 257202Generated: October 30, 2026

Tin tetrachloride → 1-(3-Methoxythiophen-2-yl)-3-methylbut-2-en-1-one

https://huagongshe.com/reaction/257202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTin tetrachlorideHCID 24287—
Reactant3-Methyl-2-butenoyl chlorideHCID 102394—
Reactant3-MethoxythiopheneHCID 140249—
ReactantPotassium BromideHCID 253877—
SolventDichloromethaneHCID 6344—
Product1-(3-Methoxythiophen-2-yl)-3-methylbut-2-en-1-oneHCID 15643882—

Reaction Steps

A solution of 3-methoxythiophene (21.3 g, 0.187 mol) [S. Gronowitz, Arkiv. Kemi., 1958, 12, 239] in dichloromethane (50 mL) was slowly added to a solution of 3,3-dimethylacryloyl chloride (22 mL, 0.195 mol) and tin(IV) chloride (23 mL, 0.195 mol) in dichloromethane (350 mL) at 0°-5° C. After stirring at 0°-5° C. an additional 1 h, the solution was poured into ice water (1 L). The organic layer was separated, washed with water, and dried over magnesium sulfate. The solvent was evaporated in vacuo. The resulting oil was purified by flash chromatography using dichloromethane as the eluant to give the product, 29.6 g (81%): mp 49°-51° C.; IR (KBr): 1671, 1628 and 1430 cm-1 ; MS: m/z 197 (MH+); 1H NMR (CDCl3): δ1.98 (d, J=1.2 Hz, 3H), 2.23 (d, J=1.1 Hz, 3H), 3.98 (s, 3H), 6.85 (d, J=5.5 Hz, 1H), 6.89 (dd, J=1.1 Hz, J=1.2 Hz, 1H) and 7.47 (d, J=5.5 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260453
Source datasetuspto-grants-1993_11
ORD IDord-7bff982e4be24299aa5a03eb268fb72f
Source noteuspto-grants-1993_11