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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969542Generated: November 3, 2026

Methanesulfonyl chloride → HCID 58557176, compound

https://huagongshe.com/reaction/1969542

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 58557598HCID 58557598—
SolventDichloromethaneHCID 6344—
ProductHCID 58557176HCID 58557176100%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of tert-butyl 2-ethyl-4-(hydroxymethyl)cyclopentanecarboxylate (0.220 g, 0.964 mmol) in DCM (5 mL) was added TEA (0.16 mL, 1.15 mmol) and methanesulfonyl chloride (0.083 mL, 1.06 mmol) at about 0° C. The reaction mixture was allowed to warm to about 25° C. and stirred at about 25° C. for about 16 h. The reaction mixture was partitioned between water (20 mL) and DCM (20 mL). The aqueous solution was washed with DCM (2×20 mL). The combined organic extracts were dried over anhydrous MgSO4, filtered, and concd under reduced pressure to give tert-butyl 2-ethyl-4-((methylsulfonyloxy)methyl)cyclopentanecarboxylate (0.295 g, 100%): LC/MS (Table 1, Method b) Rt=2.55 min; MS m/z: 307 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426411B2
Source datasetuspto-grants-2013_04
ORD IDord-9d39f83b89d547429bbd5bddcd692722
Source noteuspto-grants-2013_04