Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1944712Generated: November 1, 2026

Isobutyl chloroformate → HCID 178462117, compound

https://huagongshe.com/reaction/1944712

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsobutyl chloroformateHCID 62365—
Reactant1-Phenethylamine, (+)-HCID 643189—
ReactantHCID 178453972HCID 178453972—
SolventTetrahydrofuranHCID 8028—
SolventTriethylamineHCID 8471—
ProductHCID 178462117HCID 178462117—

Reaction Conditions

Temperature0 °C

Reaction Steps

Trans-4-tert-butoxycarbonylamino-cyclohexanecarboxylic acid (5 g, 20.5 mmol) was dissolved in THF, to which triethylamine (3 mL) was added. The reaction mixture was cooled to 0° C. and a solution of isobutyl chloroformate (2.8 g, 20.7 mmol) in THF was added dropwise. The resulting white suspension was stirred at room temperature for 30 min, after which a solution of (R)-1-phenylethanamine (2.9 g, 20.5 mmol) in THF was added dropwise. The reaction mixture was then stirred at room temperature for 4 h, after which LC-MS showed one major peak corresponding to desired product. The reaction mixture was concentrated, and the residue was diluted with water (250 mL). The resulting white precipitate was filtered, washing with ether, to afford a dry white solid tert-butyl trans-4-((R)-1-phenylethylcarbamoyl)cyclohexylcarbamate (5.2 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394858B2
Source datasetuspto-grants-2013_03
ORD IDord-4abcc8f9aef84b2a987e264251fd4f00
Source noteuspto-grants-2013_03