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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964193Generated: October 26, 2026

Benzyl Alcohol → 2,2-Dimethyl-4-benzyloxycarbonylbutyric acid

https://huagongshe.com/reaction/964193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantSulfuric AcidHCID 1118—
Reactant2,2-Dimethylglutaric acidHCID 12681—
ReactantDihydro-3,3-dimethyl-2H-pyran-2,6(3H)-dioneHCID 76247—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
Product2,2-Dimethyl-4-benzyloxycarbonylbutyric acidHCID 1908004573.6%

Reaction Steps

To a mixture of 3 g (0.021 mol) of 2.2-dimethylglutaric anhydride, 2.0 ml (0.019 mol) of benzyl alcohol in 10 ml of CH2Cl2 was added 100 mg of DMAP and 3.4 ml of pyridine. The resulting solution was stired at room temperature for 4 h. After additional 2.2-dimethyl-glutaric acid (0.7 g, 4.9 mmol) was added, the mixture continued to be stirred overnight, then poured into 0.5M H2SO4 (aq.) solution and extracted with CH2Cl2. The organic layer was washed with brine, dried over Na2SO4 and filtered. Concentration followed by purification by flash chromatography on silica gel using EtOAc/hexane (1:1) as the irrigant gave 3.5 g of desired product in 66% yield and 1.2 g of isomer in 23% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05767256
Source datasetuspto-grants-1998_06
ORD IDord-42e4ecca3cde4cb382cfced4daddbcd4
Source noteuspto-grants-1998_06