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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Tetramethoxypropane | HCID 66019 | — |
| Reactant | (Trifluoromethylthio)acetonitrile | HCID 12513752 | — |
| Catalyst | Zincchloride | HCID 3007855 | — |
| Product | 1-Cyano-1-trifluoromethylthio-4-methoxy-1,3-butadiene | HCID 53920219 | 25.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04234590 |
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| Source dataset | uspto-grants-1980_11 |
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| ORD ID | ord-9be0e4705d01431e9f19f1347d5df9ff |
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| Source note | uspto-grants-1980_11 |
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