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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888352Generated: October 31, 2026

Triethylamine → 2-Benzyloxycarbamoyl-4-methylpentanoic acid ethyl ester

https://huagongshe.com/reaction/1888352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBenzylhydroxylamineHCID 2794173—
Reactant2-(Ethoxycarbonyl)-4-methylpentanoic acidHCID 10103941—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product2-Benzyloxycarbamoyl-4-methylpentanoic acid ethyl esterHCID 1040213894.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

Intermediate (3a) (40.3 g, 214 mmol, 1.0 eq) was dissolved into 800 mL DCM and 900 mL THF and the solution was cooled to 0° C. To this was added benzyl hydroxylamine (34.2 g, 214 mmol, 1.0 eq) followed by HOBt (28.9 g, 214 mmol, 1.0 eq). The mixture was stirred for 5 minutes, then DCC (44.1 g, 214 mmol, 1.0 eq) was added, followed by triethylamine (33.4 mL, 240 mmol, 1.1 eq). The mixture was warmed to room temperature and stirred overnight. The solid was filtered and the filtrate was concentrated. The material was redissolved in 1000 mL EtOAc and washed with 500 mL 1N HCl, 600 mL saturated aq. bicarbonate, dried over MgSO4, filtered. and evaporated to yield intermediate (3b) (59.3 g) as a semisolid. MS m/z: [M+H+] calcd for C16H23NO4 294.2. found 294.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501798B2
Source datasetuspto-grants-2013_08
ORD IDord-d685b7da514c457791bf5c62b668595e
Source noteuspto-grants-2013_08