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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 587122Generated: October 29, 2026

Triethylamine → HCID 71239712, compound

https://huagongshe.com/reaction/587122

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 19804848HCID 19804848—
SolventDichloromethaneHCID 6344—
ProductHCID 71239712HCID 7123971296.9%

Reaction Conditions

Temperature-15 °C

Reaction Steps

To a solution of 4-(benzyloxy)cyclohexanecarboxylic acid (5.4 g, 23 mmol, 1.0 equiv) and triethylamine (4.82 mL, 34.57 mmol, 1.5 equiv) in DCM (dry, 40 mL) was added ethyl chloroformate (3.0 mL, 31.1 mmol, 1.35 equiv) dropwise between −20 and −10° C. under N2. The white precipitate appeared. The mixture was stirred at about −15° C. for 10 min, dried NH3 was bubbled rapidly into the liquid for 20 min. The mixture was stirred at −15° C. for 30 min, then put into the fridge (−20° C.) overnight. The flask was released the pressure and warm to room temperature. H2O (100 mL) was added. The layer was separated and the aqueous phase was extracted with DCM (3×100 mL). The combined organic solution was washed with brine (50 mL), dried over anhydrous Na2SO4, concentrated to give 5.2 g (96.7%) of 4-(benzyloxy)cyclohexanecarboxamide as a off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09226923B2
Source datasetuspto-grants-2016_01
ORD IDord-bb5d09f9f3984a20b1bdf23031a2cc74
Source noteuspto-grants-2016_01