tert-butyl 3-(2-methyl-4-(morpholinomethyl)phenoxy)azetidine-1-carboxylate

Base Information

Chemical Name:tert-butyl 3-(2-methyl-4-(morpholinomethyl)phenoxy)azetidine-1-carboxylate
CAS No.:1354792-36-1
Molecular Formula:C₂₀H₃₀N₂O₄
Molecular Weight:362.469
Hs Code.:

Synonyms:tert-butyl 3-(2-methyl-4-(morpholinomethyl)phenoxy)azetidine-1-carboxylate

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Chemical Property of tert-butyl 3-(2-methyl-4-(morpholinomethyl)phenoxy)azetidine-1-carboxylate

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Technology Process of tert-butyl 3-(2-methyl-4-(morpholinomethyl)phenoxy)azetidine-1-carboxylate

There total 1 articles about tert-butyl 3-(2-methyl-4-(morpholinomethyl)phenoxy)azetidine-1-carboxylate 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: 75.0%

: 917229-66-4
2-methyl-4-(morpholin-4-ylmethyl)phenol

: 141699-58-3
3-methanesulfonyloxy-azetidine-1-carboxylic acid tert-butyl ester

: 1354792-36-1
tert-butyl 3-(2-methyl-4-(morpholinomethyl)phenoxy)azetidine-1-carboxylate

Guidance literature:: 2-methyl-4-(morpholin-4-ylmethyl)phenol; With sodium hydride; In N,N-dimethyl-formamide; mineral oil; for 1.16667h; Inert atmosphere; Cooling with ice;

3-methanesulfonyloxy-azetidine-1-carboxylic acid tert-butyl ester; In N,N-dimethyl-formamide; mineral oil; at 80 ℃; Inert atmosphere;

Reference yield: 96.0%

: 1354792-36-1
tert-butyl 3-(2-methyl-4-(morpholinomethyl)phenoxy)azetidine-1-carboxylate

: 1354792-37-2
4-(4-(Azetidin-3-yloxy)-3-methylbenzyl)morpholine

Guidance literature:: tert-butyl 3-(2-methyl-4-(morpholinomethyl)phenoxy)azetidine-1-carboxylate; With hydrogenchloride; methanol; at 20 ℃;

With potassium carbonate; In dichloromethane; water; ethyl acetate;

Reference yield:

: 1354792-36-1
tert-butyl 3-(2-methyl-4-(morpholinomethyl)phenoxy)azetidine-1-carboxylate

: 1354791-32-4
(5-(4-methoxyphenyl)-1,3,4-oxadiazol-2-yl)(3-(2-methyl-4-(morpholinomethyl)phenoxy)-azetidin-1-yl)methanone

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride; methanol / 20 °C

2: 3 h / 120 °C

With hydrogenchloride; methanol;