(1S,2S,4R,6S)-7-benzoyl-4-methoxy-2-methyl-3-oxa-7-azabicyclo(4.2.0)octan-8-one

Base Information

Chemical Name:(1S,2S,4R,6S)-7-benzoyl-4-methoxy-2-methyl-3-oxa-7-azabicyclo(4.2.0)octan-8-one
CAS No.:115133-12-5
Molecular Formula:C₁₅H₁₇NO₄
Molecular Weight:275.304
Hs Code.:

Synonyms:(1S,2S,4R,6S)-7-benzoyl-4-methoxy-2-methyl-3-oxa-7-azabicyclo(4.2.0)octan-8-one

Suppliers and Price of (1S,2S,4R,6S)-7-benzoyl-4-methoxy-2-methyl-3-oxa-7-azabicyclo(4.2.0)octan-8-one

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Chemical Property of (1S,2S,4R,6S)-7-benzoyl-4-methoxy-2-methyl-3-oxa-7-azabicyclo(4.2.0)octan-8-one

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Technology Process of (1S,2S,4R,6S)-7-benzoyl-4-methoxy-2-methyl-3-oxa-7-azabicyclo(4.2.0)octan-8-one

There total 12 articles about (1S,2S,4R,6S)-7-benzoyl-4-methoxy-2-methyl-3-oxa-7-azabicyclo(4.2.0)octan-8-one 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: 98.0%

: 98-88-4
benzoyl chloride

: 115184-80-0
(1S,2S,4R,6S)-4-methoxy-2-methyl-3-oxa-7-azabicyclo(4.2.0)octan-8-one

: 115133-12-5
(1S,2S,4R,6S)-7-benzoyl-4-methoxy-2-methyl-3-oxa-7-azabicyclo(4.2.0)octan-8-one

Guidance literature:: With dmap; triethylamine; In dichloromethane; for 15h; Heating;
DOI:10.1016/0040-4020(89)80126-7

Reference yield:

: 115133-11-4
(1S,2S,4R,6S)-4-methoxy-7-(4-methoxyphenyl)-2-methyl-3-oxa-7-azabicyclo(4.2.0)octan-8-one

: 115133-12-5
(1S,2S,4R,6S)-7-benzoyl-4-methoxy-2-methyl-3-oxa-7-azabicyclo(4.2.0)octan-8-one

Guidance literature:: Multi-step reaction with 2 steps

1: 78 percent / ceric ammonium nitrate / acetonitrile; H₂O

2: 98 percent / Et₃N, 4-DMAP / CH₂Cl₂

With dmap; ammonium cerium(IV) nitrate; triethylamine; In dichloromethane; water; acetonitrile;
DOI:10.1016/S0040-4039(00)96544-4

Reference yield:

: 115133-09-0
(1S,2S,4R,5R)-4-hydroxy-6-(4-methoxyphenyl)-2-methyl-3-oxa-6-azabicyclo(3.2.0)heptan-7-one

: 115133-12-5
(1S,2S,4R,6S)-7-benzoyl-4-methoxy-2-methyl-3-oxa-7-azabicyclo(4.2.0)octan-8-one

Guidance literature:: Multi-step reaction with 4 steps

1: 85 percent / lithium diisopropylamide

2: 98 percent / Dowex-50(H+) / methanol

3: 78 percent / ceric ammonium nitrate / acetonitrile; H₂O

4: 98 percent / Et₃N, 4-DMAP / CH₂Cl₂

With dmap; ammonium cerium(IV) nitrate; DOWEX-50(H+); triethylamine; lithium diisopropyl amide; In methanol; dichloromethane; water; acetonitrile;
DOI:10.1016/S0040-4039(00)96544-4