HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2055208Generated: November 2, 2026
Methyl chloroformate → HCID 45095662, compound
https://huagongshe.com/reaction/2055208
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl chloroformate | HCID 6586 | — |
| Reactant | Methyl 4-ethylcyclohexane-1-carboxylate | HCID 15032104 | — |
| Reactant | Lithium diisopropylamine | HCID 45051747 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 45095662 | HCID 45095662 | 100.2% |
Reaction Steps
A solution of 4-ethyl-cyclohexanecarboxylic acid methyl ester (10.4 g, 61.2 mmol) in THF (25 mL) was added dropwise to a solution of lithium diisopropylamine (11.2 g, 92 mmol) in THF (90 mL) at −78° C. After stirring for 1 h at the same temperature, a solution of methylchloroformate (8.7 g, 92 mmol) in THF (25 mL) was added slowly and the mixture was allowed to warm to room temperature. After 18 h the reaction mixture was quenched with saturated aqueous NH4Cl solution (150 mL). THF was removed in vacuo and the aqueous residue was extracted with EtOAc (200 mL×3). The combined organic layers were dried (MgSO4). After removal of the solvent under reduced pressure, purification by flash column chromatography using an eluting system of hexane/EtOAc (95:5) yielded the title compound as a colorless liquid (14 g) with diisopropyl-carbamic acid methyl ester present. MH+229.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07332485B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-4039eddd777840f8978f219032b73cbe |
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| Source note | uspto-grants-2008_02 |
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