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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291518Generated: November 1, 2026

Triethylamine → HCID 88630703, compound

https://huagongshe.com/reaction/2291518

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantHCID 6994493HCID 6994493—
ReactantHCID 19849204HCID 19849204—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 88630703HCID 88630703—

Reaction Conditions

Temperature-10 °C

Reaction Steps

Under anhydrous conditions, to a mixture of 1.7 g (8.9 mmole) of N-t-Boc-D-alanine obtained in Part A, 1.98 g (19 mmole) triethylamine and 40 ml of tetrahydrofuran, cooled to -10° C. is added dropwise 0.96 g (8.9 mmole) ethyl chloroformate and the resulting mixture is stirred at this temperature for 20 minutes. To this is added 1.1 g (7.5 mmole) of mixed cis- and trans-isomers of 4-amino-3,5-dimethyl-1,2-dithiolane and the resulting mixture is stirred at -10° C. for 10 minutes, then allowed to warm to room temperature. The reaction mixture is diluted with water and extracted with ethyl acetate. The organic layer is washed with sodium bicarbonate solution, dilute hydrochloric acid, water, brine, then dried (Na2SO4) and the solvent is evaporated at reduced pressure to obtain the desired product which is used in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04797298
Source datasetuspto-grants-1989_01
ORD IDord-1ec7b07d24d64e15a90a4e13b050b5f2
Source noteuspto-grants-1989_01