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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1679706Generated: October 31, 2026

Allyl bromide → HCID 12395567, compound

https://huagongshe.com/reaction/1679706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant1,2-DimethoxyethaneHCID 8071—
ReactantSodium hydrideHCID 24758—
Reactant2-Methyl-5-methoxy-6,7-dichloro-1-indanoneHCID 12395561—
ProductHCID 12395567HCID 12395567—

Reaction Steps

2-Allyl-2-methyl-5-methoxy-6,7-dichloro-1-indanone is prepared following substantially the same procedure described in Example 5, Step E, using the following substances: 2-methyl-5-methoxy-6,7-dichloro-1-indanone (14.7 g., 0.06 mole), sodium hydride (1.7 g., 0.072 mole), 1,2-dimethoxyethane (500 ml.) and allyl bromide (8 ml.). The above procedure gives 11.0 g. of 2-allyl-2-methyl-5-methoxy-6,7-dichloro-1-indanone which after recrystallization from methyl cyclohexane melts at 58° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04081554
Source datasetuspto-grants-1978_03
ORD IDord-b446b96c030341be9b763d4562048854
Source noteuspto-grants-1978_03