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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2109344Generated: October 30, 2026

HCID 57519123, compound → HCID 57519124, compound

https://huagongshe.com/reaction/2109344

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57519123HCID 57519123—
CatalystBenzylidene(dichloro)(1,3-dimesitylimidazolidin-2-id-2-yl)(tricyclohexylphosphoranyl)rutheniumHCID 12045765—
SolventDichloromethaneHCID 6344—
ProductHCID 57519124HCID 5751912496%

Reaction Conditions

Temperature45 °C

Reaction Steps

To a solution of t-butyl allyl-[3-(t-butyl-diphenyl-silanyloxy)-1-(4-dimethylcarbamoyloxy-2-vinyl-phenyl)-propyl]-carbamate (360 mg, 0.56 mmol) synthesized in step (j) of Example 192 in dichloromethane (40 ml) was added tricyclohexylphosphine [1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidene] [benzylidene] ruthenium (IV) dichloride (47.5 mg, 0.0560 mmol), and the resulting mixture was stirred for 3 hours at 45° C. under a nitrogen atmosphere. After stirring, the reaction mixture was evaporated in vacuo, and the residue was purified by chromatography on a silica gel column using a mixed solvent of hexane and ethyl acetate (5:1-2:1) as the eluent to afford the title compound (330 mg, yield: 96%) as a colorless oil

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514475B2
Source datasetuspto-grants-2009_04
ORD IDord-cf2680e3414b42aea478c0a7ccb1f962
Source noteuspto-grants-2009_04