HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 656495Generated: November 2, 2026
Methyl chloroformate → HCID 66915470, compound
https://huagongshe.com/reaction/656495
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Lithium diisopropylamide | HCID 2724682 | — |
| Reactant | HCID 12119814 | HCID 12119814 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66915470 | HCID 66915470 | — |
Reaction Steps
A solution of 1 mmol of 1-benzyl-3-(2,4-dimethoxy-phenyl)-piperidin-2-one [597553-90-7] in 20 ml of tetrahydrofuran is cooled to −70° C. and treated drop wise with a solution of 1.2 mmol of lithium diisopropyl-amide in 5 ml of tetrahydrofuran. The mixture is stirred 15 minutes at −70° C. A solution of 1.2 mmol of methyl chloroformate in 5 ml of tetrahydrofuran is added at −70° C. and the reaction mixture is allowed to come to room temperature over a period of 7 hours. The reaction mixture is quenched with water and extracted with tert-butyl methyl ether (3×). The combined organic phases are dried with sodium sulphate and evaporated. From the residue the title compound is identified by means of flash chromatography (SiO2 60F) on the basis of the Rf value.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08071774B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-1143ed24f2e04ebeac7a9b6b3764332e |
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| Source note | uspto-grants-2011_12 |
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