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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 425796Generated: October 30, 2026

Dimethyl Sulfoxide → (1S,2S,5R)-2-formyl-7-methyl-3-aza-bicyclo[3.3.0]-octane-3-carboxylic acid tert.-butyl ester

https://huagongshe.com/reaction/425796

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfoxideHCID 679—
ReactantOxalyl chlorideHCID 65578—
ReactantDiisopropylethylamineHCID 81531—
Reactant(1S,2S,5R)-2-hydroxymethyl-7-methyl-3-aza-bicyclo[3.3.0]-octane-3-carboxylic acid tert.-butyl esterHCID 66703846—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product(1S,2S,5R)-2-formyl-7-methyl-3-aza-bicyclo[3.3.0]-octane-3-carboxylic acid tert.-butyl esterHCID 86643542—

Reaction Steps

To a cold (−60° C.) solution of oxalyl chloride (0.081 mL, 1.2 eq) in dry DCM (2.2 mL) was added dropwise a solution of DMSO (0.13 mL, 2.2 eq) in dry DCM (1.7 mL) within 4 min. After 10 min, was added dropwise (1S,2S,5R)-2-hydroxymethyl-7-methyl-3-aza-bicyclo[3.3.0]-octane-3-carboxylic acid tert.-butyl ester (206 mg) in dry DCM (1.2 mL) during 5 min. After 2 min a white suspension was formed. Stirring was continued 30 min at −55° C., then DIPEA (0.690 mL, 5 eq) (which was dried over 3A M.S.) was added during 3-4 min. The reaction mixture was allowed to come to RT, diluted with water and extracted with DCM. The combined org. extracts were washed with citric acid (5%), brine, dried over anh. MgSO4, filtered and evaporated to yield the title compound as an oil, which was used for the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08106215B2
Source datasetuspto-grants-2012_01
ORD IDord-90a6390a916b42539bec1d8bbd43bad4
Source noteuspto-grants-2012_01