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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 931722Generated: October 31, 2026

(S)-2-tert-butoxy-2-(7-chloro-5-(4-chlorophenyl)-2-methylquinolin-6-yl)ethanol → (S)-2-tert-butoxy-2-(5-(4-chlorophenyl)-7-methylquinolin-6-yl)ethanol

https://huagongshe.com/reaction/931722

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-tert-butoxy-2-(7-chloro-5-(4-chlorophenyl)-2-methylquinolin-6-yl)ethanolHCID 66631657—
Reactant(S)-2-tert-butoxy-2-(5-(4-chlorophenyl)-7-methylquinolin-6-yl)ethyl pivalateHCID 66631713—
Product(S)-2-tert-butoxy-2-(5-(4-chlorophenyl)-7-methylquinolin-6-yl)ethanolHCID 66631592—

Reaction Steps

Compound 3K was prepared following the procedure used to prepare compound 1K of example 1, except that (S)-2-tert-butoxy-2-(5-(4-chlorophenyl)-7-methylquinolin-6-yl)ethyl pivalate (3J) was used instead of compound 1J. LCMS-ESI+ (m/z): 370.2, 372.2 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296758B2
Source datasetuspto-grants-2016_03
ORD IDord-c0daf7d462f2456aa8f371f895425fae
Source noteuspto-grants-2016_03