methyl (1'R,3'R)-2-benzyloxycarbonylamino-3-[2',2'-dimethyl-3'-(2-methyl-1,3-dioxolan-2-yl)cyclobutyl]-(Z)-2-propenoate

Base Information

Chemical Name:methyl (1'R,3'R)-2-benzyloxycarbonylamino-3-[2',2'-dimethyl-3'-(2-methyl-1,3-dioxolan-2-yl)cyclobutyl]-(Z)-2-propenoate
CAS No.:288848-45-3
Molecular Formula:C₂₂H₂₉NO₆
Molecular Weight:403.475
Hs Code.:

Synonyms:methyl (1'R,3'R)-2-benzyloxycarbonylamino-3-[2',2'-dimethyl-3'-(2-methyl-1,3-dioxolan-2-yl)cyclobutyl]-(Z)-2-propenoate

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Chemical Property of methyl (1'R,3'R)-2-benzyloxycarbonylamino-3-[2',2'-dimethyl-3'-(2-methyl-1,3-dioxolan-2-yl)cyclobutyl]-(Z)-2-propenoate

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Technology Process of methyl (1'R,3'R)-2-benzyloxycarbonylamino-3-[2',2'-dimethyl-3'-(2-methyl-1,3-dioxolan-2-yl)cyclobutyl]-(Z)-2-propenoate

There total 5 articles about methyl (1'R,3'R)-2-benzyloxycarbonylamino-3-[2',2'-dimethyl-3'-(2-methyl-1,3-dioxolan-2-yl)cyclobutyl]-(Z)-2-propenoate 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: 50.0%

: 100945-15-1,88568-95-0
N-(benzyloxycarbonyl)phosphonoglycine trimethyl ester

: 288848-39-5
(1S,3R)-2,2-dimethyl-3-(2-methyl-1,3-dioxolan-2-yl)cyclobutanocarbaldehyde

: 288848-45-3
methyl (1'R,3'R)-2-benzyloxycarbonylamino-3-[2',2'-dimethyl-3'-(2-methyl-1,3-dioxolan-2-yl)cyclobutyl]-(Z)-2-propenoate

Guidance literature:: With potassium tert-butylate; In dichloromethane; at 20 ℃; for 54h;
DOI:10.1021/jo991773c

Reference yield:

: 288848-24-8
(1S,3R)-3-acetyl-2,2-dimethylcyclobutane carboxylic acid

: 288848-45-3
methyl (1'R,3'R)-2-benzyloxycarbonylamino-3-[2',2'-dimethyl-3'-(2-methyl-1,3-dioxolan-2-yl)cyclobutyl]-(Z)-2-propenoate

Guidance literature:: Multi-step reaction with 5 steps

1: 98 percent / KOH / diethyl ether; ethanol / 1 h / 20 °C

2: 90 percent / pyridinium p-toluenesulfonate / benzene / 4 h / Heating

3: 95 percent / LiBH₄ / tetrahydrofuran / Heating

4: 74 percent / PDC / CH₂Cl₂ / 4 h / 20 °C

5: 50 percent / t-BuOK / CH₂Cl₂ / 54 h / 20 °C

With potassium hydroxide; dipyridinium dichromate; lithium borohydride; potassium tert-butylate; pyridinium p-toluenesulfonate; In tetrahydrofuran; diethyl ether; ethanol; dichloromethane; benzene; 1: Methylation / 2: ketal formation / 3: Reduction / 4: Oxidation / 5: Condensation;
DOI:10.1021/jo991773c

Reference yield:

: 136780-45-5
methyl (1S,3R)-3-acetyl-2,2-dimethylcyclobutanecarboxylate

: 288848-45-3
methyl (1'R,3'R)-2-benzyloxycarbonylamino-3-[2',2'-dimethyl-3'-(2-methyl-1,3-dioxolan-2-yl)cyclobutyl]-(Z)-2-propenoate

Guidance literature:: Multi-step reaction with 4 steps

1: 90 percent / pyridinium p-toluenesulfonate / benzene / 4 h / Heating

2: 95 percent / LiBH₄ / tetrahydrofuran / Heating

3: 74 percent / PDC / CH₂Cl₂ / 4 h / 20 °C

4: 50 percent / t-BuOK / CH₂Cl₂ / 54 h / 20 °C

With dipyridinium dichromate; lithium borohydride; potassium tert-butylate; pyridinium p-toluenesulfonate; In tetrahydrofuran; dichloromethane; benzene; 1: ketal formation / 2: Reduction / 3: Oxidation / 4: Condensation;
DOI:10.1021/jo991773c