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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712793Generated: October 29, 2026

HCID 72270955, compound → HCID 72270946, compound

https://huagongshe.com/reaction/712793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 72270955HCID 72270955—
CatalystHCID 178479819HCID 178479819—
SolventDichloromethaneHCID 6344—
ProductHCID 72270946HCID 72270946132%

Reaction Steps

To a solution of N-allyl-N-(1-((tert-butyldiphenylsilyl)oxy)pent-4-en-2-yl)-4-methylbenzenesulfonamide (D10) (7.12 g, 13.33 mmol) in DCM (64 ml), Grubb's catalyst (1.09 g, 1.32 mmol) was added and the mixture was stirred at RT overnight. After solvent evaporation, the residue was loaded on KP-Si (100 g) cartridge eluting with a mixture cHex/EtOAc from 100/0 to 90/10. Collected fractions after solvent evaporation afforded the title compound (D11) (8.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181279B2
Source datasetuspto-grants-2015_11
ORD IDord-61be521c72594d4daf7dd0aab939fdec
Source noteuspto-grants-2015_11