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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 629695Generated: October 27, 2026

Dimethyl Sulfoxide → Tert-butyl (2S,5S)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2-formylmorpholine-4-carboxylate

https://huagongshe.com/reaction/629695

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantTriethylamineHCID 8471—
ReactantOxalyl chlorideHCID 65578—
ReactantTert-butyl (2S,5S)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2-(hydroxymethyl)morpholine-4-carboxylateHCID 86726301—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductTert-butyl (2S,5S)-5-(((tert-butyldimethylsilyl)oxy)methyl)-2-formylmorpholine-4-carboxylateHCID 86726303—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of oxalyl chloride (2 eq) in DCM (0.3 M) at −78° C. was added a solution of DMSO (5 eq) in DCM (0.5M). The reaction mixture was stirred at −78° C. for 30 min. A solution of tert-butyl (2S,5S)-5-({[tert-butyl(dimethyl)silyl]oxy}methyl)-2-(hydroxymethyl)morpholine-4-carboxylate (1 eq) in CH2Cl2 (0.2M) was added dropwise and stirred at −40° C. for 1.5 hours. It was then cooled to −78° C. and triethylamine (7 eq) was added and the reaction mixture was stirred at 0° C. for 1 h. Water was added and the reaction mixture was warmed to rt for 30 min. The mixture was diluted with CH2Cl2, the organic layer was washed with water and brine, dried over Na2SO4, filtered and concentrated. The crude product was used as such for the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09315475B2
Source datasetuspto-grants-2016_04
ORD IDord-4eb63425462545c59f4669ca39e92ca9
Source noteuspto-grants-2016_04