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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655273Generated: October 26, 2026

Triethylamine → HCID 15646116, compound

https://huagongshe.com/reaction/1655273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactantpsi-PelletierineHCID 11096—
Reactant2,2,2-Trichloroethyl chloroformateHCID 87063—
CatalystPotassium CarbonateHCID 11430—
SolventHydrochloric AcidHCID 313—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 15646116HCID 1564611676.1%

Reaction Steps

To a solution of pseudopelletierine (52 g, 0.34 mol) in toluene (220 mL) at 50° C. was added anhydrous potassium carbonate (1.0 g), followed by the slow addition of trichloroethylchloroformate (79 g, 0.37 mol). After addition was completed (30 minutes), triethylamine (10 mL) was added. The reaction was allowed to cool to room temperature and stirred for 18 hours. The reaction mixture was diluted with ethyl acetate (300 mL) and 1N hydrochloric acid (200 mL). After the organic layer was washed with 1N hydrochloric acid (100 mL), it was washed with aqueous 10% sodium hydroxide (100 mL). The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated to afford a beige solid which was triturated with hexane (300 mL) to afford 81.4 g of crystalline solid (76% yield); mp 95°-96° C. after recrystallization from ethyl acetate-hexane. Anal. (C11H14C13NO3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250537
Source datasetuspto-grants-1993_10
ORD IDord-5ebd17a7ebf543f2aa6fdad6211aef7d
Source noteuspto-grants-1993_10