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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264378Generated: October 31, 2026

Oxalyl chloride → HCID 86584828, compound

https://huagongshe.com/reaction/1264378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantTrimethylsilyldiazomethaneHCID 167693—
ReactantHCID 69431236HCID 69431236—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventHexaneHCID 8058—
ProductHCID 86584828HCID 8658482848%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 25 g (93 mmol) (2S,4R)-1-Methanesulfonyl-4-tritylsulfanyl-pyrrolidine-2-carboxylic acid in 265 ml CH2Cl2 at 0° C. was treated with 2 drops of DMF followed by 8 ml (99 mmol) oxalylchloride. After 15 min at 0° C. the reaction was stirred 2 h at RT, evaporated and dissolved in 260 ml THF/CH3CN 1:1. 58.5 ml (117 mmol) 2M trimethylsilyldiazomethane solution in hexane was then added at 0° C.. The reaction was stirred 16h at RT, evaporated and poured in H2O/EtOAc. The organic phase was dried over Na2SO4, evaporated and purified by flash column chromatography on silicagel with hexane/EtOAc (7:3 to 1:1) to give 12.4 g (48%) of (2S,4R)-2-Diazo-1-(1-methanesulfonyl-4-tritylsulfanyl-pyrrolidin-2-yl)-ethanone, MS: 509 (MNH4+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541638B2
Source datasetuspto-grants-2003_04
ORD IDord-5204cca35add4598b2190a31a470cba6
Source noteuspto-grants-2003_04