HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 231336Generated: October 31, 2026
Chlorotrimethylsilane → HCID 53876422, compound
https://huagongshe.com/reaction/231336
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 54071723 | HCID 54071723 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 53876422 | HCID 53876422 | 84.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04845257 |
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| Source dataset | uspto-grants-1989_07 |
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| ORD ID | ord-b596f37403494467875489c317fba76c |
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| Source note | uspto-grants-1989_07 |
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