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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231336Generated: October 31, 2026

Chlorotrimethylsilane → HCID 53876422, compound

https://huagongshe.com/reaction/231336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorotrimethylsilaneHCID 6397—
ReactantTriethylamineHCID 8471—
ReactantHCID 54071723HCID 54071723—
SolventAcetonitrileHCID 6342—
ProductHCID 53876422HCID 5387642284.1%

Reaction Conditions

Temperature-30 °C

Reaction Steps

In 15 ml of acetonitrile was dissolved 795 mg of methyl 2-methoxyimino-3-oxobutyrate, followed by addition of 2.1 ml of triethylamine. Then, 1.9 ml of chlorotrimethylsilane was added dropwise with ice-cooling and the mixture was stirred at 20°-25° C. for 1 hour for silylation. The reaction mixture was concentrated under reduced pressure and the residue was suspended in 15 ml of tetrahydrofuran. The suspension was filtered in a nitrogen gas stream to remove insolubles. The filtrate was cooled to -30° C. and 0.405 ml of sulfuryl chloride was added dropwise. After the temperature of the system was increased to 20° C., the mixture was concentrated under reduced pressure. The concentrate was chromatographed on a silica gel column and elution was carried out with 100 ml of hexane-ether (1:1, v/v). The eluate was concentrated under reduced pressure to give 813 mg of methyl 4-chloro-2-methoxyimino-3-oxobutyrate as colorless oil. Yield 84.1%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04845257
Source datasetuspto-grants-1989_07
ORD IDord-b596f37403494467875489c317fba76c
Source noteuspto-grants-1989_07