Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1434447Generated: October 31, 2026

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

https://huagongshe.com/reaction/1434447

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 numberUS07612114B2
Source datasetuspto-grants-2009_11
ORD IDord-44727933037a4946915cbf35f11978f0
Source noteuspto-grants-2009_11