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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1180442Generated: November 1, 2026

Triethylamine → HCID 86605382, compound

https://huagongshe.com/reaction/1180442

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantLeucic acid, L-HCID 83697—
ReactantSodium BicarbonateHCID 516892—
ReactantAminoacetonitrile hydrochlorideHCID 11491918—
SolventDimethylformamideHCID 6228—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 86605382HCID 86605382—

Reaction Conditions

Temperature0 °C

Reaction Steps

L-leucic acid (85 g, 0.643 mole), amino acetonitrile hydrochloride (68 g, 0.734 mole, 1.14 eg), pyBOP (319 g, 0.612 mole, 0.95 eg) were mixed together in DMF (1 L) and cooled at 0° C. Triethylamine (149 g, 1.47 mole, 2.4 eg) was added dropwise at a rate to maintain internal temperature ≦20° C. Reaction mixture was then allowed to warm to room temperature and stirred for 18 hours. Reaction mixture was poured portionwise into saturated NaHCO3 (4 L) and extracted with EtOAc (2×1 L). Half saturated NaCl solution was added to help partition. Combined organic fractions were washed with brine, 0.5 N HCl, brine, dried and evaporated to give a dark red oil. The latter was passed through a silica plug with 50% EtOAc/hexane to give of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07279478B2
Source datasetuspto-grants-2007_10
ORD IDord-45c0a8ce5ce0442d91c2be7ad1a2d3cb
Source noteuspto-grants-2007_10