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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757201Generated: October 31, 2026

Trifluoromethanesulfonic anhydride → methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate

https://huagongshe.com/reaction/1757201

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoromethanesulfonic anhydrideHCID 67749—
ReactantSodium BicarbonateHCID 516892—
ReactantMethyl 6'-Desmethyl-4'-tosylmycophenolateHCID 10672181—
SolventDichloromethaneHCID 6344—
Productmethyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoateHCID 10555649—

Reaction Steps

Trifluoromethanesulfonic anhydride (10.57 g) was added to a solution of methyl (E) 6-(1,3-dihydro-6-hydroxy-7-methyl-3-oxo-4-p-toluenesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate in methylene chloride (500 ml) amd pyridine (5 ml) at 0° C. After 6 hours the reaction was added to excess aqueous sodium bicarbonate. The organic solution was dried and evaporated to afford methyl (E) 6-(1,3-dihydro-7-methyl-3-oxo-4-p-toluenesulfonyloxy-6-trifluoromethanesulfonyloxyisobenzofuran-5-yl)-4-methyl-4-hexenoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05444072
Source datasetuspto-grants-1995_08
ORD IDord-bf0888ef069f4d12874fcbf9aca3f94e
Source noteuspto-grants-1995_08