tert-butyl (4-(4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl)butyl)carbamate

Base Information

Chemical Name:tert-butyl (4-(4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl)butyl)carbamate
CAS No.:1610591-74-6
Molecular Formula:C₂₀H₃₁ClN₂O₃
Molecular Weight:382.931
Hs Code.:

Synonyms:tert-butyl (4-(4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl)butyl)carbamate

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Chemical Property of tert-butyl (4-(4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl)butyl)carbamate

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Technology Process of tert-butyl (4-(4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl)butyl)carbamate

There total 3 articles about tert-butyl (4-(4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl)butyl)carbamate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 51.0%

: 39512-49-7
4-(4-chlorophenyl)-4-hydroxypiperidine

: 174626-25-6
methanesulfonic acid 4-tert-butoxycarbonylaminobutyl ester

: 1610591-74-6
tert-butyl (4-(4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl)butyl)carbamate

Guidance literature:: In acetonitrile; for 22h; Reflux;
DOI:10.1021/jm500457x

Reference yield:

: 24424-99-5
di-tert-butyl dicarbonate

: 1610591-74-6
tert-butyl (4-(4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl)butyl)carbamate

Guidance literature:: Multi-step reaction with 3 steps

1: triethylamine / dichloromethane / 1 h / 20 °C

2: triethylamine / dichloromethane / 0 - 20 °C

3: acetonitrile / 22 h / Reflux

With triethylamine; In dichloromethane; acetonitrile;
DOI:10.1021/jm500457x

Reference yield:

: 75178-87-9
(4-hydroxybutyl)carbamic acid tert-butyl ester

: 1610591-74-6
tert-butyl (4-(4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl)butyl)carbamate

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 0 - 20 °C

2: acetonitrile / 22 h / Reflux

With triethylamine; In dichloromethane; acetonitrile;
DOI:10.1021/jm500457x