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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917995Generated: November 1, 2026

Trimethylsilyldiazomethane → HCID 53710760, compound

https://huagongshe.com/reaction/1917995

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyldiazomethaneHCID 167693—
Reactant4,4,4-Trifluoro-3-oxobutanenitrileHCID 13843540—
SolventDiethyl EtherHCID 3283—
ProductHCID 53710760HCID 53710760—

Reaction Conditions

Temperature0 °C

Reaction Steps

(Trimethylsilyl)diazomethane (21 mL, 2M in diethyl ether) was added dropwise to a solution of 4,4,4-trifluoro-3-oxobutanenitrile (3.79 g, 26 mmol) in anhydrous diethyl ether (25 mL) previously cooled to 0° C. The resulting mixture was allowed to slowly warm to room temperature and stirred overnight. The solvent was removed under reduced pressure to give 4,4,4-trifluoro-3-methoxybut-2-enenitrile, which was directly used in the next step without further purification. 1H NMR (300 MHz, CDCl3) d 5.00 (s, 1H), 4.16 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618289B2
Source datasetuspto-grants-2013_12
ORD IDord-1a3d0d6a777e40c696a03b3f0edbbc22
Source noteuspto-grants-2013_12