HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1879028Generated: November 1, 2026
Methyl chloroformate → HCID 67533511, compound
https://huagongshe.com/reaction/1879028
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 57448065 | HCID 57448065 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67533511 | HCID 67533511 | 55.8% |
Reaction Steps
To a solution of 4-[2-fluoro-3-(methylthio)phenyl]-1,2,3,6-tetrahydropyridine (1.35 g, 6.05 mmol) and triethyl amine (1.2 ml, 7.2 mmol) in methylen chloride (20 ml) at 0° C., a solution of methyl chloroformate (0.49 g, 6.6 mmol) in methylen chloride (5 ml), was added dropwise. The mixture was stirred for 15 min at 0° C. and for 1 h at ambient temperature. The reaction was quenched with aqueous sodium carbonate (10%, 50 ml), the phases were separated and the aqueous phase was extracted with methylen chloride (3×50 ml). The combined organic phases was dried (MgSO4), filtered and evaporated to dryness to give the title compound (0.95 g). MS m/z (rel. intensity, 70 eV) 281 (M+, 65), 267 (16), 266 (bp), 147 (27), 146 (25).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08314126B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-fd72b68a5a144479b347157ccd8a64d5 |
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| Source note | uspto-grants-2012_11 |
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