Triisopropyl-((1R,2R,4S)-2-methoxy-4-{(2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-4-[2-((E)-(R)-1-methyl-3-(R)-oxiranyl-but-2-enyl)-[1,3]dithian-2-yl]-butyl}-cyclohexyloxy)-silane

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Chemical Name:Triisopropyl-((1R,2R,4S)-2-methoxy-4-{(2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-4-[2-((E)-(R)-1-methyl-3-(R)-oxiranyl-but-2-enyl)-[1,3]dithian-2-yl]-butyl}-cyclohexyloxy)-silane
CAS No.:186448-86-2
Molecular Formula:C₄₀H₆₈O₅S₂Si
Molecular Weight:721.194
Hs Code.:

Triisopropyl-((1R,2R,4S)-2-methoxy-4-{(2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-4-[2-((E)-(R)-1-methyl-3-(R)-oxiranyl-but-2-enyl)-[1,3]dithian-2-yl]-butyl}-cyclohexyloxy)-silane

Synonyms:Triisopropyl-((1R,2R,4S)-2-methoxy-4-{(2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-4-[2-((E)-(R)-1-methyl-3-(R)-oxiranyl-but-2-enyl)-[1,3]dithian-2-yl]-butyl}-cyclohexyloxy)-silane

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Chemical Property of Triisopropyl-((1R,2R,4S)-2-methoxy-4-{(2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-4-[2-((E)-(R)-1-methyl-3-(R)-oxiranyl-but-2-enyl)-[1,3]dithian-2-yl]-butyl}-cyclohexyloxy)-silane

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Technology Process of Triisopropyl-((1R,2R,4S)-2-methoxy-4-{(2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-4-[2-((E)-(R)-1-methyl-3-(R)-oxiranyl-but-2-enyl)-[1,3]dithian-2-yl]-butyl}-cyclohexyloxy)-silane

There total 14 articles about Triisopropyl-((1R,2R,4S)-2-methoxy-4-{(2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-4-[2-((E)-(R)-1-methyl-3-(R)-oxiranyl-but-2-enyl)-[1,3]dithian-2-yl]-butyl}-cyclohexyloxy)-silane 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:

: 186448-81-7
Toluene-4-sulfonic acid (E)-(2R,5R)-2-hydroxy-5-{2-[(2S,3R)-2-(4-methoxy-benzyloxy)-4-((1S,3R,4R)-3-methoxy-4-triisopropylsilanyloxy-cyclohexyl)-3-methyl-butyl]-[1,3]dithian-2-yl}-3-methyl-hex-3-enyl ester

: 186448-86-2
Triisopropyl-((1R,2R,4S)-2-methoxy-4-{(2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-4-[2-((E)-(R)-1-methyl-3-(R)-oxiranyl-but-2-enyl)-[1,3]dithian-2-yl]-butyl}-cyclohexyloxy)-silane

Guidance literature:: With potassium carbonate; In methanol; for 1h; Ambient temperature;
DOI:10.1021/ja963066w

Reference yield:

: 89238-99-3
O-(4-methoxybenzyl)-trichloroacetimidate

: 186448-86-2
Triisopropyl-((1R,2R,4S)-2-methoxy-4-{(2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-4-[2-((E)-(R)-1-methyl-3-(R)-oxiranyl-but-2-enyl)-[1,3]dithian-2-yl]-butyl}-cyclohexyloxy)-silane

Guidance literature:: Multi-step reaction with 5 steps

1: 84 percent / BF₃*Et₂O / CH₂Cl₂ / -78 °C

2: 87 percent / t-BuLi / hexamethylphosphoric acid triamide; tetrahydrofuran / -78 °C

3: 73 percent / camphorsulfonic acid / methanol / 2 h / Ambient temperature

4: 85 percent / Et₃N, DMAP / CH₂Cl₂ / 16 h / Ambient temperature

5: K₂CO₃ / methanol / 1 h / Ambient temperature

With dmap; camphor-10-sulfonic acid; boron trifluoride diethyl etherate; tert.-butyl lithium; potassium carbonate; triethylamine; In tetrahydrofuran; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; dichloromethane;
DOI:10.1021/ja963066w

Reference yield:

: 127258-23-5
(1R,2R,4R)-4-<(phenylsulfonyl)methyl>-2-methoxy-1-<oxy>cyclohexane

: 186448-86-2
Triisopropyl-((1R,2R,4S)-2-methoxy-4-{(2R,3S)-3-(4-methoxy-benzyloxy)-2-methyl-4-[2-((E)-(R)-1-methyl-3-(R)-oxiranyl-but-2-enyl)-[1,3]dithian-2-yl]-butyl}-cyclohexyloxy)-silane

Guidance literature:: Multi-step reaction with 9 steps

1: 1.) n-BuLi, 2.) BF₃*Et₂O, 3.) Na₂HPO₄, 4.) Na(Hg)

2: 92 percent / Et₃N

3: 87 percent / NaH / hexamethylphosphoric acid triamide / 6 h / Ambient temperature

4: 78 percent / LiI, BF₃*OEt₂ / diethyl ether / -78 °C

5: 84 percent / BF₃*Et₂O / CH₂Cl₂ / -78 °C

6: 87 percent / t-BuLi / hexamethylphosphoric acid triamide; tetrahydrofuran / -78 °C

7: 73 percent / camphorsulfonic acid / methanol / 2 h / Ambient temperature

8: 85 percent / Et₃N, DMAP / CH₂Cl₂ / 16 h / Ambient temperature

9: K₂CO₃ / methanol / 1 h / Ambient temperature

With dmap; disodium hydrogenphosphate; n-butyllithium; sodium amalgam; camphor-10-sulfonic acid; boron trifluoride diethyl etherate; tert.-butyl lithium; sodium hydride; potassium carbonate; triethylamine; lithium iodide; In tetrahydrofuran; methanol; N,N,N,N,N,N-hexamethylphosphoric triamide; diethyl ether; dichloromethane;
DOI:10.1021/ja963066w