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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 855320Generated: October 25, 2026

Dichloromethane → 4-(1,1-Dimethyl-but-3-enyl)-benzoic acid methyl ester

https://huagongshe.com/reaction/855320

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantAllyltrimethylsilaneHCID 69808—
Reactant4-(1-Methoxy-1-methyl-ethyl)-benzoic acid methyl esterHCID 18174485—
CatalystTitanium TetrachlorideHCID 24193—
Product4-(1,1-Dimethyl-but-3-enyl)-benzoic acid methyl esterHCID 6934308938%

Reaction Conditions

Temperature-78 °C

Reaction Steps

827 mg of 4-(1-methoxy-1-methyl-ethyl)-benzoic acid methyl ester (3.97 mmol) (prepared as described in example S102) and 1.26 ml allyltrimethylsilane (7.94 mmol) were dissolved in 10 ml DCM and the solution was cooled to −78° C. Then 4.77 ml of a 1 M solution of TiCl4 in DCM were added dropwise. After 30 h the reaction was quenched at −78° C. by addition of methanol. Then water was added and the mixture was extracted 3 times with DCM. The combined extracts were washed with brine, dried with magnesium sulfate, filtered and concentrated. The remaining residue was purified by chromatography (silica gel; cyclohexane/EtOAc 95:5) to give 331 mg (38%) of 4-(1,1-dimethyl-but-3-enyl)-benzoic acid methyl ester as a colorless liquid. 1H NMR (CDCl3, 300 MHz): δ 1.33 (s, 6H), 2.38 (d, J=7 Hz, 2H), 3.90 (s, 3H), 4.91-5.00 (m, 3H), 5.51 (m, 1H), 7.41 (d, J=9 Hz, 1H), 7.97 (d, J=9 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259183B2
Source datasetuspto-grants-2007_08
ORD IDord-7452562ce91a4b45a012e10bbdf46c86
Source noteuspto-grants-2007_08