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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2230434Generated: November 1, 2026

Dimethyl Sulfoxide → t-Butyl N-Allyloxycarbonyl-4-amino-5-oxopentanoate

https://huagongshe.com/reaction/2230434

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactantt-Butyl N-allyloxycarbonyl-4-amino-5-hydroxypentanoateHCID 18465850—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Productt-Butyl N-Allyloxycarbonyl-4-amino-5-oxopentanoateHCID 18465646—

Reaction Conditions

Temperature-70 °C

Reaction Steps

To a solution of DMSO (1.51 g, 19.3 mmol) in CH2Cl2 (25 ml) at −70° C. was added oxalyl chloride (1.34 g, 19.3 mmol). After 10 minutes at −70° C., a solution of (206a) (2.4 g, 8.8 mmol) in CH2Cl2 (10 ml) was added dropwise and the mixture stirred for 15 minutes at −70° C. Diisopropylethylamine (3.4 g, 26.3 mmol) was added and the mixture stirred at −25° C. for 15 minutes then diluting with EtOAc (50 ml) washed with a solution of sodium hydrogen sulfate 2M, concentrated to give an oil which was used immediately without purification: 1H NMR (CDCl3) δ9.5 (1H, s), 6.0-5.5 (2H, m), 5.5-5.1 (2H, m), 4.5 (2H, m), 4.2 (1H, m), 2.4-2.10 (2H, m), 2.05 (2H, m), 1.36 (9H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06423840B1
Source datasetuspto-grants-2002_07
ORD IDord-72c7b77761624d43be748fab8fcdeec4
Source noteuspto-grants-2002_07