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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 742352Generated: October 30, 2026

methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate → methyl (E) 6-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate

https://huagongshe.com/reaction/742352

Reaction equation

Participants

RoleNameHCIDCharge
Reactantmethyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoateHCID 10672508—
CatalystTrichlororhodium;tris(triphenylphosphane)HCID 157991709—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
Productmethyl (E) 6-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoateHCID 10696303—

Reaction Steps

A solution of methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-vinylisobenzofuran-5-yl)-4-methyl-4-hexenoate (17.7 g) and tris(triphenylphosphine) rhodium chloride (1.2 g) in benzene (180 ml) and ethanol (180 ml) was hydrogenated for 11 hours. The solvents were removed under vacuum and the residue was crystallized from ethyl acetate/tert butyl methyl ether to afford methyl (E) 6-(1,3-dihydro-6-ethyl-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate, mp 101.3°-102.08° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05554612
Source datasetuspto-grants-1996_09
ORD IDord-dd1068850ba044b0aa3724fd21affc9a
Source noteuspto-grants-1996_09