C₂₈H₃₆O₇

Base Information Edit

Chemical Name:C₂₈H₃₆O₇
CAS No.:82770-03-4
Molecular Formula:C₂₈H₃₆O₇
Molecular Weight:484.59
Hs Code.:
Mol file:82770-03-4.mol

C<sub>28</sub>H<sub>36</sub>O<sub>7</sub>

Synonyms:C₂₈H₃₆O₇

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Chemical Property of C₂₈H₃₆O₇ Edit

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Technology Process of C₂₈H₃₆O₇

There total 7 articles about C₂₈H₃₆O₇ 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:

: 82769-84-4,82769-85-5
((S)-1-Phenyl-ethyl)-carbamic acid 2,2,3a,7-tetramethyl-5-phenylsulfanyl-hexahydro-benzo[1,3]dioxol-4-yl ester

: 82770-03-4
C₂₈H₃₆O₇

Guidance literature:: Multi-step reaction with 6 steps

1: 15.0 g / m-chloroperbenzoic acid / CH₂Cl₂ / 1.) -35 deg C, 10 min, 2.) -35 deg C -> 25 deg C, 1 h

2: 1,8-diazabicyclo<5.4.0>undec-7-ene / tetrahydrofuran / Heating

3: 1.) KDA / 1.) THF, 40 min, 2.) -25 deg C, 30 min

4: 1.) potassium tert-butoxide, 2.) ammoniua, lithium / 1.) tert-butyl alcohol, THF, 0 deg C, 5 min, 2.) -78 deg C, 1.5 h

6: 1.) 80percent m-chloroperbenzoic acid, sodium bicarbonate / 1.) methylene chloride, 0 deg C, 25 min, 2.) pyridine, 25 deg C, 3 h

With Diethoxy-methyl-(6-amino-hexylaminomethyl)-silan; potassium tert-butylate; ammonia; lithium; sodium hydrogencarbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; dichloromethane;
DOI:10.1021/ja00385a030

Reference yield:

: 82769-87-7
(1'S,1R,2R,3S,4S,6R)-2,6-dimethyl-3-<(((1'-phenylethyl)amino)carbonyl)oxy>-4-(phenylsulfonyl)cyclohexane-1,2-diol 1,2-acetonide

: 82770-03-4
C₂₈H₃₆O₇

Guidance literature:: Multi-step reaction with 5 steps

1: 1,8-diazabicyclo<5.4.0>undec-7-ene / tetrahydrofuran / Heating

2: 1.) KDA / 1.) THF, 40 min, 2.) -25 deg C, 30 min

3: 1.) potassium tert-butoxide, 2.) ammoniua, lithium / 1.) tert-butyl alcohol, THF, 0 deg C, 5 min, 2.) -78 deg C, 1.5 h

5: 1.) 80percent m-chloroperbenzoic acid, sodium bicarbonate / 1.) methylene chloride, 0 deg C, 25 min, 2.) pyridine, 25 deg C, 3 h

With Diethoxy-methyl-(6-amino-hexylaminomethyl)-silan; potassium tert-butylate; ammonia; lithium; sodium hydrogencarbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran;
DOI:10.1021/ja00385a030

Reference yield:

: 82796-49-4
(1R,2S,6R)-2,6-dimethyl-4-(phenylsulfonyl)cyclohex-3-ene-1,2-diol 1,2-diacetonide

: 82770-03-4
C₂₈H₃₆O₇

Guidance literature:: Multi-step reaction with 4 steps

1: 1.) KDA / 1.) THF, 40 min, 2.) -25 deg C, 30 min

2: 1.) potassium tert-butoxide, 2.) ammoniua, lithium / 1.) tert-butyl alcohol, THF, 0 deg C, 5 min, 2.) -78 deg C, 1.5 h

4: 1.) 80percent m-chloroperbenzoic acid, sodium bicarbonate / 1.) methylene chloride, 0 deg C, 25 min, 2.) pyridine, 25 deg C, 3 h

With Diethoxy-methyl-(6-amino-hexylaminomethyl)-silan; potassium tert-butylate; ammonia; lithium; sodium hydrogencarbonate; 3-chloro-benzenecarboperoxoic acid;
DOI:10.1021/ja00385a030