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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1374407Generated: October 31, 2026

Triethylamine → HCID 86592518, compound

https://huagongshe.com/reaction/1374407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantEthyl chloroformateHCID 10928—
ReactantSodium borohydrideHCID 4311764—
Reactant51644-83-8HCID 6992708—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86592518HCID 8659251850%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of N-(benzyloxy)carbonyl-D-glutamic acid 5-tert-butyl ester (35 g, 102 mol) in THF (500 ml) was added at −30° C. triethylamine (17 ml, 122 mmol), followed by addition of ethyl chloroformate (12 ml, 122 mmol) and the mixture was stirred at the same temperature. Then to the mixture was added at −30° C. a solution of sodium borohydride (11.6 g, 306 mmol) in water (51 ml) and the mixture was stirred for 30 minutes. Then the solution was raised to 0° C. and stirred for 30 minutes. To the reaction mixture was added water and the solution was extracted three times with ethyl acetate and the organic layer was washed with a saturated aqueous sodium chloride solution, dried over magnesium sulfate and the organic solvent was removed under reduced pressure. The residue was purified by silica gel (210 g) chromatography (Hexane/ethyl acetate: 3/2→1/1) to give tert-butyl (4R)-4-{[(benzyloxy)carbonyl]amino}-5-hydroxypentanoate (16.5 g, 50%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163936B2
Source datasetuspto-grants-2007_01
ORD IDord-41fc72d95ae84f75a7abb0e09d4bc577
Source noteuspto-grants-2007_01