(R)-1-isopropoxycarbonylbenzyl (1R,2R)-1-benzamido-2-phenylcyclopropanecarboxylate

Base Information

Chemical Name:(R)-1-isopropoxycarbonylbenzyl (1R,2R)-1-benzamido-2-phenylcyclopropanecarboxylate
CAS No.:161904-86-5
Molecular Formula:C₂₈H₂₇NO₅
Molecular Weight:457.526
Hs Code.:

Synonyms:(R)-1-isopropoxycarbonylbenzyl (1R,2R)-1-benzamido-2-phenylcyclopropanecarboxylate

Suppliers and Price of (R)-1-isopropoxycarbonylbenzyl (1R,2R)-1-benzamido-2-phenylcyclopropanecarboxylate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Total 1 raw suppliers

Chemical Property of (R)-1-isopropoxycarbonylbenzyl (1R,2R)-1-benzamido-2-phenylcyclopropanecarboxylate

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

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Technology Process of (R)-1-isopropoxycarbonylbenzyl (1R,2R)-1-benzamido-2-phenylcyclopropanecarboxylate

There total 4 articles about (R)-1-isopropoxycarbonylbenzyl (1R,2R)-1-benzamido-2-phenylcyclopropanecarboxylate 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: 80.0%

: 161793-81-3
(R)-1-isopropoxycarbonylbenzyl (3S,4S)-3-benzamido-4-phenyl-1-pyrazoline-3-carboxylate

: 161904-86-5
(R)-1-isopropoxycarbonylbenzyl (1R,2R)-1-benzamido-2-phenylcyclopropanecarboxylate

Guidance literature:: In benzene; for 6h; Irradiation;
DOI:10.1016/S0040-4020(01)89550-8

Reference yield:

: 89015-27-0
(R)-α-hydroxyphenylacetic acid iso-propyl ester

: 161904-86-5
(R)-1-isopropoxycarbonylbenzyl (1R,2R)-1-benzamido-2-phenylcyclopropanecarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 70 percent / p-TsOH*H₂O / tetrahydrofuran / 24 h / Heating

2: 33 percent / diethyl ether / 120 h / 0 °C

3: 80 percent / benzene / 6 h / Irradiation

With toluene-4-sulfonic acid; In tetrahydrofuran; diethyl ether; benzene;
DOI:10.1016/S0040-4020(01)89550-8

Reference yield:

: 17606-70-1,5839-91-8
(4Z)-4-benzylidene-2-phenyl-1,3-oxazol-5(4H)-one

: 161904-86-5
(R)-1-isopropoxycarbonylbenzyl (1R,2R)-1-benzamido-2-phenylcyclopropanecarboxylate

Guidance literature:: Multi-step reaction with 3 steps

1: 70 percent / p-TsOH*H₂O / tetrahydrofuran / 24 h / Heating

2: 33 percent / diethyl ether / 120 h / 0 °C

3: 80 percent / benzene / 6 h / Irradiation

With toluene-4-sulfonic acid; In tetrahydrofuran; diethyl ether; benzene;
DOI:10.1016/S0040-4020(01)89550-8