C₃₈H₄₈N₂O₈

Base Information

Chemical Name:C₃₈H₄₈N₂O₈
CAS No.:1025986-24-6
Molecular Formula:C₃₈H₄₈N₂O₈
Molecular Weight:660.808
Hs Code.:

C<sub>38</sub>H<sub>48</sub>N<sub>2</sub>O<sub>8</sub>

Synonyms:

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Chemical Property of C₃₈H₄₈N₂O₈

Chemical Property:

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Technology Process of C₃₈H₄₈N₂O₈

There total 7 articles about C₃₈H₄₈N₂O₈ 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:

: 3978-80-1
Boc-Tyr-OH

: 1025986-24-6
C₃₈H₄₈N₂O₈

Guidance literature:: Multi-step reaction with 8 steps

1: 82 percent / LiAlH₄ / diethyl ether

2: 87 percent / p-toluenesulfonic acid / acetone

3: 82 percent / DCC, DMAP

4: 64 percent / Tebbe's reagent / toluene

5: 46 percent / toluene / 120 °C

6: DDQ

7: NaBH₄ / methanol

8: 1.) thiocarbonyl diimidazole, DMAP, 2.) n-Bu₃SnH, AIBN / 2.) toluene

With dmap; sodium tetrahydroborate; lithium aluminium tetrahydride; Tebbe's reagent; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; toluene-4-sulfonic acid; di(1H-imidazol-2-yl)methanethione; dicyclohexyl-carbodiimide; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In methanol; diethyl ether; acetone; toluene;
DOI:10.1021/jo00048a005

Reference yield:

: 83345-46-4,282100-80-5
N-(tert-butyloxycarbonyl)-L-tyrosinol

: 1025986-24-6
C₃₈H₄₈N₂O₈

Guidance literature:: Multi-step reaction with 7 steps

1: 87 percent / p-toluenesulfonic acid / acetone

2: 82 percent / DCC, DMAP

3: 64 percent / Tebbe's reagent / toluene

4: 46 percent / toluene / 120 °C

5: DDQ

6: NaBH₄ / methanol

7: 1.) thiocarbonyl diimidazole, DMAP, 2.) n-Bu₃SnH, AIBN / 2.) toluene

With dmap; sodium tetrahydroborate; Tebbe's reagent; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; toluene-4-sulfonic acid; di(1H-imidazol-2-yl)methanethione; dicyclohexyl-carbodiimide; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In methanol; acetone; toluene;
DOI:10.1021/jo00048a005

Reference yield:

: 143817-60-1
(4S)-3-(tert-Butyloxycarbonyl)-2,2-dimethyl-4-<<4-(3-methoxy-1,3-butadien-2-oxy)phenyl>methyl>oxazolidine

: 1025986-24-6
C₃₈H₄₈N₂O₈

Guidance literature:: Multi-step reaction with 4 steps

1: 46 percent / toluene / 120 °C

2: DDQ

3: NaBH₄ / methanol

4: 1.) thiocarbonyl diimidazole, DMAP, 2.) n-Bu₃SnH, AIBN / 2.) toluene

With dmap; sodium tetrahydroborate; 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; di(1H-imidazol-2-yl)methanethione; 2,3-dicyano-5,6-dichloro-p-benzoquinone; In methanol; toluene;
DOI:10.1021/jo00048a005