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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2392735Generated: October 30, 2026

3-Chloro-2-methyl-1-propene → HCID 18980411, compound

https://huagongshe.com/reaction/2392735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2-methyl-1-propeneHCID 11241—
Reactant3-BromophenolHCID 11563—
ReactantHCID 10999837HCID 10999837—
Reactant192870-97-6HCID 15816719—
ProductHCID 18980411HCID 1898041133%

Reaction Steps

1-bromo-3-(2-methyl-allyloxy)-benzene, prepared by the alkylation of 1-bromo-3-hydroxy-benzene with 3-chloro-2-methyl-1-propene, was reacted with 4-benzyloxy-2-dimethylaminomethyl-cyclohexanone corresponding to the conditions described in Example 1. The base obtained was purified with 9:1 ether/methanol via a silica gel column, taken up in ether and treated with trimethylchlorosilane/water. Compound (4) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05801201
Source datasetuspto-grants-1998_09
ORD IDord-d96830ea5d4340359f0ccf24bf704218
Source noteuspto-grants-1998_09