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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2115614Generated: October 26, 2026

Methanol → Isobutyric acid 4-(tert-butyl-diphenyl-silanyloxy)-but-2-enyl ester

https://huagongshe.com/reaction/2115614

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantIsobutyryl chlorideHCID 62325—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(tert-Butyl-diphenyl-silanyloxy)-but-2-en-1-olHCID 66656949—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductIsobutyric acid 4-(tert-butyl-diphenyl-silanyloxy)-but-2-enyl esterHCID 66656955—

Reaction Steps

Isobutyryl chloride (10.4 mL, 98.04 mmol) was added drop wise to a stirred and a cooled (0° C.) solution of the product of Example 5E (61.28 mmol), diisopropylethyl amine (21.3 mL, 122.56 mmol), and 4-dimethylaminopyridine (0.30 g, 3.0 mmol) in dry dichloromethane (150 mL). The resulting solution was allowed to stir at 0° C. for five hours. After the completion of reaction (monitored by TLC), methanol (5 mL) was added to quench excess acid chloride. The solvent was removed under reduced pressure and the resulting slurry was partitioned using diethyl ether (200 mL) and saturated NH4Cl (100 mL). The organic layer was washed successively with 20% NaHSO4, NaHCO3, brine, and it was dried over MgSO4. After removal of solvent, the crude oil was purified over silica gel column using 10% diethyl ether in hexanes to give the title compound as a colorless oil: (20.5 g, 84% over 2 steps).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435833B2
Source datasetuspto-grants-2008_10
ORD IDord-ffd1b24aa7a04628a12393bead2df428
Source noteuspto-grants-2008_10