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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 876580Generated: October 30, 2026

Dimethylformamide → HCID 67222560, compound

https://huagongshe.com/reaction/876580

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant1-(1,1-Dimethylethyl) (2R,3R)-2,3-bis(acetyloxy)butanedioateHCID 14143476—
ReactantHCID 65029835HCID 65029835—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 67222560HCID 67222560102.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of (R,R)-2,3-bis(acetyloxy)-butanedioic acid mono tert-butyl ester (3.25 g: Tetrahedron, 45, 3071-3080, 1989) in CH2Cl2 (65 mL), were added oxalyl chloride (1.06 mL) and DMF (50 microL) at 0° C. The reaction mixture was stirred at 0° C. for 30 minutes then pyridine (3.82 mL) was added into the mixture at the same temperature. The reaction mixture was stirred at the same temperature for 5 minutes. To the mixture, was added a solution of compound 54-2 (2.5 g) in CH2Cl2 (12.5 mL) at 0° C. The mixture was stirred for 1 hour at the same temperature. Then the mixture was concentrated in vacuo and the resulting residue was suspended in water. The mixture was extracted with EtOAc and the organic layer was washed with 1N HCl aq., sat. NaHCO3 aq., brine, and it was dried with anhyd. Na2SO4. The solvent was removed under reduced pressure to obtain compound 54-3 (5.7 g) as brown oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987242B2
Source datasetuspto-grants-2015_03
ORD IDord-b2e63aaab69c415a93f2fd1ba5763133
Source noteuspto-grants-2015_03