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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1086629Generated: October 30, 2026

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

https://huagongshe.com/reaction/1086629

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 numberUS05030736
Source datasetuspto-grants-1991_07
ORD IDord-e0294fd4732d4405ba58aa7485759975
Source noteuspto-grants-1991_07