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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1854582Generated: October 30, 2026

tert-Butyl acetate → Tert-butyl 2-(2-chloro-5-isopropyl-phenyl)acetate

https://huagongshe.com/reaction/1854582

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl acetateHCID 10908—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant3-Bromo-4-chloroisopropylbenzeneHCID 50997864—
CatalystTris(1,1-dimethylethyl)phosphineHCID 83681—
Catalyst(1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladiumHCID 6505921—
SolventTolueneHCID 1140—
SolventDiethyl EtherHCID 3283—
ProductTert-butyl 2-(2-chloro-5-isopropyl-phenyl)acetateHCID 11772057990.4%

Reaction Steps

Add bis(dibenzylideneacetone)palladium (49.2 mg, 85.6 μmol) to a round bottom flask and seal with a septum. Flush with nitrogen. Add tri-tert-butylphosphine (85.6 μL, 85.6 μmol, 1M in toluene) and lithium bis(trimethylsilyl)amide (12.8 mL, 11.56 mmol, 0.9M in methylcyclohexanes) via a syringe. Add 2-bromo-1-chloro-4-isopropyl-benzene (1.0 g, 4.28 mmol) and t-butyl acetate (865.2 μL, 6.42 mmol) via a syringe. Add toluene (10.7 mL) via a syringe and the reaction mixture becomes hot to the touch. Place on an ambient temperature water bath and stir for 3 hours. Store the reaction mixture in the freezer over the weekend. Warm the reaction mixture to ambient temperature. Dilute the reaction mixture with diethyl ether and add saturated ammonium chloride solution. Separate the layers and wash the diethyl ether layer with saturated sodium chloride solution. Dry over sodium sulfate, filter and concentrate under reduced pressure. Purify the residue by silica gel chromatography eluting with acetone: hexanes (0-2% gradient) to give the title compound (1.04 g). Purify again by silica gel chromatography eluting with dichloromethane: hexanes (0-20% gradient) to give the title compound (490 mg, 1.82 mmol). MS (m/z): 213.0 (M-tBu+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962654B2
Source datasetuspto-grants-2015_02
ORD IDord-4f15eebe23404caf92548f6ab4a0f95c
Source noteuspto-grants-2015_02