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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 448194Generated: October 30, 2026

Benzyl bromoacetate → HCID 68769595, compound

https://huagongshe.com/reaction/448194

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl bromoacetateHCID 62576—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 68738533HCID 68738533—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ProductHCID 68769595HCID 68769595—

Reaction Conditions

Temperature-65 °C

Reaction Steps

To a stirred solution of 3-Acetylphenyl 2,6-dimethylbenzoate (Step B, 2.90 g, 10.8 mmol) in dry THF (50 ml) and DMPU (17 ml) was added a solution of lithium bis(trimethylsilyl) amide (1.0M, 11.89 ml) at −65° C. under argon. After 10 minutes of stirring at −65° C., benzyl bromoacetate (3.72 g, 16.24 mmol) was added rapidly. The reaction mixture was stirred for an additional 10 minutes and then warmed to room temperature for 4 hours. The crude mixture was taken in ethyl acetate and washed with water and brine. The aqueous layer was extracted one more time with ethyl acetate. The combined organic layers were dried over Na2SO4, filtered, concentrated and purified by flash chromatography on a silica gel column (hex: ethyl acetate, 4:1) to provide the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481595B2
Source datasetuspto-grants-2013_07
ORD IDord-03224fd78dd9415c83c019b6039707eb
Source noteuspto-grants-2013_07