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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446947Generated: October 29, 2026

Triethylamine → ((R)-1-dimethylcarbamoyl-3-methyl-butyl)-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/446947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantDimethylamine, hydrochlorideHCID 10473—
ReactantPyBOPHCID 2724699—
ReactantBOC-D-LEU-OH H2OHCID 2724763—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product((R)-1-dimethylcarbamoyl-3-methyl-butyl)-carbamic acid tert-butyl esterHCID 2816566158%

Reaction Steps

To a solution of Boc-D-leucine monohydrate (2.0 g, 8.0 mmol), triethylamine (5.6 mL, 40.1 mmol), and dimethylamine hydrochloride (1.31 g, 16.0 mmol) in DMF (15 mL) at room temperature was added PyBOP (4.59 g, 8.82 mmol). The reaction mixture was stirred overnight then diluted with EtOAc (50 mL) and washed with water (4×50 mL). The combined organic extracts were dried (Na2SO4) and evaporated under vacuum. The crude residue was purified by SiO2 chromatography (80 g, hexanes/EtOAc, 1:1) to give 1.19 g (58%) of ((R)-1-dimethylcarbamoyl-3-methyl-butyl)-carbamic acid tert-butyl ester as a colorless viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481541B2
Source datasetuspto-grants-2013_07
ORD IDord-948d16f949124e3abb92073d9e0fda0f
Source noteuspto-grants-2013_07