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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1592366Generated: November 3, 2026

Ethanol → Boc-D-alanine Ethyl Ester

https://huagongshe.com/reaction/1592366

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantBOC-D-alanineHCID 637606—
Catalyst2-DimethylaminopyridineHCID 21885—
SolventDichloromethaneHCID 6344—
ProductBoc-D-alanine Ethyl EsterHCID 1251502885.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Boc-D-alanine (5.0 g, 26.4 mmol), dimethylaminopyridine (161 mg, 1.3 mMol), and ethanol (1.34 g, 29.1 mMol) were dissolved in methylene chloride (300 ml), and the solution was cooled to 0° C. To this solution was added 1,3-dicyclohexylcarbodiimide (6.0 g, 29.1 mMol). The mixture was allowed to slowly come to room temperature, and stirred under nitrogen overnight, during which time a white solid precipitated. The precipitate was removed by filtration, rinsed with methylene chloride, and the filtrate was concentrated to a pale yellow oil. Flash chromatography in 10-30% EtOAc/Hexanes yielded 4.9 g of a colorless oil as product. NMR (300 MHz, CDCl3) δ 5.05 (b, 1H), 4.28 (q, 1H, J=7 Hz), 4.20 (q, 2H, J=7 Hz), 1.45 (s, 9H), 1.38 (d, 3H, J=7 Hz), 1.28 (t, 3H, J=7 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07291744B2
Source datasetuspto-grants-2007_11
ORD IDord-8cfbef61161c4f61aea8b240f554ed94
Source noteuspto-grants-2007_11