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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2424210Generated: November 1, 2026

2-Chloroethyl chloroformate → 6-[2-(2-Hydroxyethylamino)-4-methoxyphenyl]-5,6,7,8-tetrahydronaphthalen-2-ol

https://huagongshe.com/reaction/2424210

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroethyl chloroformateHCID 12305—
Reactant6-(2-Amino-4-methoxyphenyl)-5,6,7,8-tetrahydronaphthalen-2-olHCID 23087328—
SolventPyridineHCID 1049—
Product6-[2-(2-Hydroxyethylamino)-4-methoxyphenyl]-5,6,7,8-tetrahydronaphthalen-2-olHCID 57933749—

Reaction Conditions

Temperature180 °C

Reaction Steps

To a solution of 6-(2-amino-4-methoxyphenyl)-5,6,7,8-tetrahydronaphthalen-2-ol (1.6 g) in pyridine (6 ml) was added dropwise 2-chloroethyl chloroformate (1.4 ml) on an ice bath, and the solution was stirred for 6.5 hours. The solution was diluted with ice water, and then extracted with ethyl acetate. The solution was washed with brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. To the residue were added potassium hydroxide (3.0 g) and ethylene glycol (15 ml), and the solution was heated for 3 hours at 180° C. The solution was diluted with ice water, and then extracted with ethyl acetate. The solution was washed with brine, dried over anhydrous magnesium sulfate, and then the solvent was evaporated in vacuo. The residue was purified by silica gel column chromatography (hexane-ethyl acetate system) to provide the title compound (800 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960412B2
Source datasetuspto-grants-2011_06
ORD IDord-6d5eab9aa17c41b99d49786e3c6c7312
Source noteuspto-grants-2011_06