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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 276934Generated: October 30, 2026

Bromine → 1-Methoxycarbonylmethoxy-5-oxo-6-bromo-5,6,7,8-tetrahydronaphthalene

https://huagongshe.com/reaction/276934

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
Reactant1-Methoxycarbonylmethoxy-5-oxo-5,6,7,8-tetrahydronaphthaleneHCID 14181186—
SolventDichloromethaneHCID 6344—
Product1-Methoxycarbonylmethoxy-5-oxo-6-bromo-5,6,7,8-tetrahydronaphthaleneHCID 22629167—

Reaction Steps

To a solution of 1-methoxycarbonylmethoxy-5-oxo-5,6,7,8-tetrahydronaphthalene (0.5 g) in dry dichloromethane (3 ml) was added bromine (0.14 ml) at 0° C. The mixture was warmed up to room temperature, stirred for 2 hours. The mixture was washed with an aqueous saturated sodium bicarbonate, dried over magnesium sulfate and evaporated in vacuo. The residue was chromatographed on silica gel (30 ml) using a mixture of dichloromethane-n-hexane. The desired fractions were collected and evaporated in vacuo to give 1-methoxycarbonylmethoxy-5-oxo-6-bromo-5,6,7,8-tetrahydronaphthalene (0.41 g). The crude crystal (50 mg) was recrystallized from ethyl acetate-n-hexane to give 31 mg as a white crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355640B1
Source datasetuspto-grants-2002_03
ORD IDord-129f58d5aff944af92c3a54a5b479609
Source noteuspto-grants-2002_03