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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608337Generated: October 31, 2026

2-Chloroethanol → HCID 14881362, compound

https://huagongshe.com/reaction/1608337

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroethanolHCID 34—
ReactantHCID 178517341HCID 178517341—
Solventtert-ButanolHCID 6386—
SolventSodium HydroxideHCID 14798—
ProductHCID 14881362HCID 14881362102.6%

Reaction Conditions

Temperature60 °C

Reaction Steps

Ethylene chlorohydrin (9.0 g) was added to a solution of 2-hydroxy-3-(2-phenylethyl)-5,6,7,8-tetrahydro quinoxaline (5.59 g, 22 mM) in aqueous 5N NaOH and t-butanol (60 ml), and stirred at 60° C. for 3 hours. The t-butanol was distilled off in vacuo, water was added to the residue, and the mixture was extracted three times with chloroform. The extract was dried with anhydrous sodium sulfate and concentrated in vacuo. The residue was charged on a column of silica-gel (C-200, 170 g) packed with chloroform, and eluted with chloroform-methanol (200:1) to obtain compound 645 (6.73 g, yield: 90.9%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04870176
Source datasetuspto-grants-1989_09
ORD IDord-a399769d03294bb4b9d2c7e8ae6b88f7
Source noteuspto-grants-1989_09