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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 645335Generated: October 26, 2026

Dibromomethane → 1-(Cyclopropylmethyl)-4-methoxybenzene

https://huagongshe.com/reaction/645335

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDibromomethaneHCID 3024—
ReactantAcetyl chlorideHCID 6367—
ReactantEstragoleHCID 8815—
Reactanttert-Butyl methyl etherHCID 15413—
CatalystZincHCID 23994—
CatalystCuprous chlorideHCID 62652—
SolventDiethyl EtherHCID 3283—
Product1-(Cyclopropylmethyl)-4-methoxybenzeneHCID 6422476589.7%

Reaction Conditions

Temperature45 °C

Reaction Steps

CH2Br2 (220 g) was added to a slurry of zinc powder (340 g) and CuCl (54 g) in diethyl ether (450 ml). The reaction was started by the addition of acetyl chloride (8 g). The reaction mixture was heated to 45° C. and a solution of estragol (192 g) in ether (150 ml) was added during 25 minutes. Additional CH2Br2 (456 g) dissolved in ether (150 ml) was dropped into the grey-red suspension during 45 minutes. Afterwards, the mixture was stirred at 50° C. for 12 hours. The suspension was cooled to room temperature and MTBE (900 ml) was added. The mixture was filtered through celite, and the filtrate was washed with saturated NH4Cl, water, saturated NaHCO3 and brine, dried (MgSO4) and concentrated in vacuo. The residue was distilled (b.p. 90-95° C./0.1 Torr) to yield 97.5 g (46%) of a colorless oil, which was found to have the following characteristics, NMR and MS spectra.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704942B2
Source datasetuspto-grants-2010_04
ORD IDord-30f4661058b54a008d52b9a20ce7ef92
Source noteuspto-grants-2010_04