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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2390992Generated: October 27, 2026

Triethylamine → HCID 178501230, compound

https://huagongshe.com/reaction/2390992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloro-5-(trifluoromethyl)benzoyl chlorideHCID 2778106—
ReactantHCID 178501210HCID 178501210—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 178501230HCID 178501230—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred suspension of trans-4-amino-cyclohexylcarboxylic acid methyl ester hydrochloride (6.7 g, 34.7 mmol) in dry THF (90 mL) under nitrogen atmosphere is added triethylamine (12 mL, 86.8 mmol). The suspension is cooled to 0° C. and 2-chloro-5-(trifluoromethyl)benzoyl chloride (8.85 g, 36.4 mmol) in dry THF (40 mL) is added dropwise over 20 minutes. The resulting thick, colourless slurry is stirred at 0-5° C. for 30 minutes and then allowed to warm to room temp and stirred at room temp for 1 hour. The reaction is quenched by the dropwise addition of water (5 mL) in THF (45 mL) to give a clear solution. This is diluted with water (100 mL) and ethyl acetate (300 mL). The biphasic mixture is stirred for 5 minutes then the organic phase is separated and washed successively with water (100 mL), saturated sodium bicarbonate (100 mL) and saturated brine (100 mL), dried (MgSO4), filtered and evaporated to give a colourless solid.; [MH+ 364].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273900B2
Source datasetuspto-grants-2012_09
ORD IDord-a17dfab1de5a4dbcba870eedc1acbdd8
Source noteuspto-grants-2012_09