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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769647Generated: November 1, 2026

Diethyl Ether → HCID 86748409, compound

https://huagongshe.com/reaction/1769647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl EtherHCID 3283—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
Reactant(6S)-6-(Propylamino)-5,6,7,8-tetrahydronaphthalen-1-olHCID 10219902—
SolventWaterHCID 962—
ProductHCID 86748409HCID 8674840981.3%

Reaction Steps

A stirring suspension of (S)-6-propylamino-5,6,7,8-tetrahydro-l-naphthalenol (7.34 g, 0.0257 mol) in water (100 mL) was cooled in an ice bath and sodium bicarbonate (8.49 g, 0,101 mol) was added. This suspension was stirred for fifteen minutes then benzyl chloroformate (4.50 g, 0.0264 mol) was added dropwise. The mixture was stirred for fifteen minutes and then allowed to come to room temperature. Ether (100 mL) was added and the mixture was stirred overnight. The layers were separated and the aqueous layer was extracted with ether. The combined organic layers were washed twice with saturated aqueous sodium bicarbonate, once with water, twice with dilute hydrochloric acid, once with water and once with saturated aqueous sodium chloride, dried (magnesium sulfate) and concentrated under reduced pressure to give 7.09 g (81% yield) of product as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05382596
Source datasetuspto-grants-1995_01
ORD IDord-55cfc5a86d324534b531e1ad06d969f2
Source noteuspto-grants-1995_01