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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224781Generated: October 26, 2026

Acetic Anhydride → 1-Cyano-1-trifluoromethylthio-4-methoxy-1,3-butadiene

https://huagongshe.com/reaction/224781

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTetramethoxypropaneHCID 66019—
Reactant(Trifluoromethylthio)acetonitrileHCID 12513752—
CatalystZincchlorideHCID 3007855—
Product1-Cyano-1-trifluoromethylthio-4-methoxy-1,3-butadieneHCID 5392021925.3%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of acetic anhydride (52 mL), 1,1,3,3-tetramethoxypropane (26.4 g, 0.16 mL), trifluoromethylthioacetonitrile (14.5 g, 0.1 mol) and ZnCl2 (1 g) was heated at reflux. After 18 hours, the mixture was distilled up to 100° at atmospheric pressure. The residue was then cooled to 25° C. and filtered. The clear solution was distilled to yield 3.5 g of 4-cyano-4-trifluoromethylthio-3-butenealdehydedimethylacetal (bp 65°-93° C. at 18 mm) and 5.3 g of 1-cyano-1-trifluoromethylthio-4-methoxy-1,3-butadiene (bp 83°-105° C. at 0.5 mm). This material was combined and used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04234590
Source datasetuspto-grants-1980_11
ORD IDord-9be0e4705d01431e9f19f1347d5df9ff
Source noteuspto-grants-1980_11