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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 24581Generated: October 25, 2026

Chloromethyl Methyl Ether → (+/-) Ethyl 4-[(5,5-dimethyl-8-(methoxymethyloxy)-5,6,7,8-tetrahydronaphthalen-2-yl)azo]benzoate

https://huagongshe.com/reaction/24581

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloromethyl Methyl EtherHCID 7864—
ReactantIsopropylethylamineHCID 88318—
ReactantEthyl 4-[(5,5-dimethyl-8-hydroxy-5,6,7,8-tetrahydronaphthalen-2-yl)azo]benzoateHCID 22571548—
SolventDichloromethaneHCID 6344—
Product(+/-) Ethyl 4-[(5,5-dimethyl-8-(methoxymethyloxy)-5,6,7,8-tetrahydronaphthalen-2-yl)azo]benzoateHCID 22571546—

Reaction Steps

To a solution of (+1-) ethyl 4-[(5,5-dimethyl-8-hydroxy-5,6,7,8-tetrahydronaphthalen-2-yl)azo]benzoate (Compound D5, 49.7 mg, 0.141 mmol) in 4 ml of dry CH2Cl2 at 0° C. was added isopropyl ethyl amine (0.152 ml, 0.847 mmol) followed by chloromethyl methyl ether (0.0323 ml, 0.423 mmol). The reaction mixture was stirred at room temperature for 12 h. Solvent was removed under reduced pressure, the residue was dissolved in ethyl acetate and the solution was washed with NaHCO3 (sat.), and brine. The organic layer was dried (MgSO4). The solvent was removed under reduced pressure, the residue was purfied by flash chromatography (silica, ethyl acetate:hexane, 1:3) to afford the title compound as a red oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06855832B2
Source datasetuspto-grants-2005_02
ORD IDord-48e95bc7edf04fa7b722037e86cc8d02
Source noteuspto-grants-2005_02