dl-(1β,2α,3β,5β)-2-(formylmethyl)-3-<(phenylsulfonyl)amino>-6-oxabicyclo<3.1.0>hexane

Base Information

Chemical Name:dl-(1β,2α,3β,5β)-2-(formylmethyl)-3-<(phenylsulfonyl)amino>-6-oxabicyclo<3.1.0>hexane
CAS No.:123539-05-9
Molecular Formula:C₁₃H₁₅NO₄S
Molecular Weight:281.332
Hs Code.:

Synonyms:dl-(1β,2α,3β,5β)-2-(formylmethyl)-3-<(phenylsulfonyl)amino>-6-oxabicyclo<3.1.0>hexane

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Chemical Property of dl-(1β,2α,3β,5β)-2-(formylmethyl)-3-<(phenylsulfonyl)amino>-6-oxabicyclo<3.1.0>hexane

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Technology Process of dl-(1β,2α,3β,5β)-2-(formylmethyl)-3-<(phenylsulfonyl)amino>-6-oxabicyclo<3.1.0>hexane

There total 8 articles about dl-(1β,2α,3β,5β)-2-(formylmethyl)-3-<(phenylsulfonyl)amino>-6-oxabicyclo<3.1.0>hexane 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:

: 113084-34-7
dl-(1β,2α,3β,5β)-2-(hydroxyethyl)-3-<(phenylsulfonyl)amino>-6-oxabicyclo<3.1.0>hexane

: 123539-05-9
dl-(1β,2α,3β,5β)-2-(formylmethyl)-3-<(phenylsulfonyl)amino>-6-oxabicyclo<3.1.0>hexane

Guidance literature:: With oxalyl dichloride; dimethyl sulfoxide; In dichloromethane; at -60 ℃; for 0.25h;
DOI:10.1021/jm00163a038

Reference yield:

: 49826-08-6,54483-54-4,54483-55-5,75331-67-8
1-hydroxy-2-(2-hydroxyethyl)cyclopent-3-ene

: 123539-05-9
dl-(1β,2α,3β,5β)-2-(formylmethyl)-3-<(phenylsulfonyl)amino>-6-oxabicyclo<3.1.0>hexane

Guidance literature:: Multi-step reaction with 8 steps

1: 96 percent / Et₃N, 4-(dimethylamino)pyridine / CH₂Cl₂ / 20 h / Ambient temperature

2: Et₃N / CH₂Cl₂ / 0.5 h / 0 °C

3: NaN₃ / dimethylformamide / 5 h / 75 °C

4: 1.) Ph₃P, 2.) H₂O / 1.) RT, 15 h, 2.) a.) 45 deg C, 2 h, b.) reflux, 1 h

5: Et₃N / CH₂Cl₂ / 0.5 h / 0 °C

6: 99 percent / 1 N aq. HCl / tetrahydrofuran; methanol / 2 h / 45 °C

7: 22.6 percent / 80percent 3-chloroperbenzoic acid / CH₂Cl₂ / 15 h / 0 °C

8: oxalyl chloride/DMSO / CH₂Cl₂ / 0.25 h / -60 °C

With hydrogenchloride; dmap; sodium azide; oxalyl dichloride; water; dimethyl sulfoxide; triethylamine; 3-chloro-benzenecarboperoxoic acid; triphenylphosphine; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jm00163a038

Reference yield:

: 113007-91-3
dl-trans-2-<2-<(phenylsulfonyl)amino>cyclopent-4-enyl>ethanol

: 123539-05-9
dl-(1β,2α,3β,5β)-2-(formylmethyl)-3-<(phenylsulfonyl)amino>-6-oxabicyclo<3.1.0>hexane

Guidance literature:: Multi-step reaction with 2 steps

1: 22.6 percent / 80percent 3-chloroperbenzoic acid / CH₂Cl₂ / 15 h / 0 °C

2: oxalyl chloride/DMSO / CH₂Cl₂ / 0.25 h / -60 °C

With oxalyl dichloride; dimethyl sulfoxide; 3-chloro-benzenecarboperoxoic acid; In dichloromethane;
DOI:10.1021/jm00163a038