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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2176281Generated: October 29, 2026

Methanesulfonyl chloride → HCID 86706127, compound

https://huagongshe.com/reaction/2176281

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 86706128HCID 86706128—
SolventDichloromethaneHCID 6344—
ProductHCID 86706127HCID 8670612798%

Reaction Steps

Following the procedure reported in Example 84, the N-Boc group of 1-tert-butyl 4-ethyl 4-vinylpiperidine-1,4-dicarboxylate 84a (450 mg) was removed via treatment with 4N HCl in dioxane/DCM at RT for 1 h to give ethyl 4-vinylpiperidine-4-carboxylate. Ethyl 4-vinylpiperidine-4-carboxylate reacted with MsCl with TEA in DCM at RT for 18 h to give ethyl 1-(methylsulfonyl)-4-vinylpiperidine-4-carboxylate 85a (409 mg, 98% yield). LCMS [M+H]+=249.90 (-Boc); Tr=1.96 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062092B2
Source datasetuspto-grants-2015_06
ORD IDord-a91214472c2b4740ad7bd932cc660105
Source noteuspto-grants-2015_06