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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1512018Generated: November 3, 2026

L-Homoserine → HCID 131729812, compound

https://huagongshe.com/reaction/1512018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantL-HomoserineHCID 12647—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
SolventAcetonitrileHCID 6342—
ProductHCID 131729812HCID 131729812—

Reaction Steps

To a suspension of L-homoserine (1 g, 8.4 mmol) in acetonitrile (10 ml) at 0° C. was added 1,8-diazabicyclo[5.4.0]undec-7-ene (1.32 ml, 8.8 mmol, 1.05 eq). tert-butyldimethylsilyl chloride (1.33 g, 8.8 mmol, 1.05 eq) was then added portionwise over 5 minutes and the reaction mixture allowed to warm to room temperature and stirred for 16 hours. A white precipitate formed, which was filtered off and washed with acetonitrile before drying under reduced pressure. The title compound was isolated as a white solid (1.8 g, 92% yield). 1H NMR (500 MHz, DMSO-d6), δ: 7.5 (1H, br s), 3.7 (1H, m), 3.35 (4H, br m), 1.95 (1H, m), 1.70 (1H, m), 0.9 (9H, s), 0.1 (6H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08217050B2
Source datasetuspto-grants-2012_07
ORD IDord-bf7cc01357864e808d7b9f158cf716ad
Source noteuspto-grants-2012_07