(3aR,4R,5S,7aR)-4{[(1,1-dimethylethyl)diphenylsilyl]oxy}-3a,4,5,7a-tetrahydro-6-iodo-2,2-dimethyl-1,3-benzodioxol-5-ol

Base Information

Chemical Name:(3aR,4R,5S,7aR)-4{[(1,1-dimethylethyl)diphenylsilyl]oxy}-3a,4,5,7a-tetrahydro-6-iodo-2,2-dimethyl-1,3-benzodioxol-5-ol
CAS No.:231934-87-5
Molecular Formula:C₂₅H₃₁IO₄Si
Molecular Weight:550.509
Hs Code.:

Synonyms:(3aR,4R,5S,7aR)-4{[(1,1-dimethylethyl)diphenylsilyl]oxy}-3a,4,5,7a-tetrahydro-6-iodo-2,2-dimethyl-1,3-benzodioxol-5-ol

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Chemical Property of (3aR,4R,5S,7aR)-4{[(1,1-dimethylethyl)diphenylsilyl]oxy}-3a,4,5,7a-tetrahydro-6-iodo-2,2-dimethyl-1,3-benzodioxol-5-ol

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Technology Process of (3aR,4R,5S,7aR)-4{[(1,1-dimethylethyl)diphenylsilyl]oxy}-3a,4,5,7a-tetrahydro-6-iodo-2,2-dimethyl-1,3-benzodioxol-5-ol

There total 3 articles about (3aR,4R,5S,7aR)-4{[(1,1-dimethylethyl)diphenylsilyl]oxy}-3a,4,5,7a-tetrahydro-6-iodo-2,2-dimethyl-1,3-benzodioxol-5-ol 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: 85.0%

: 77-76-9
2,2-dimethoxy-propane

: 403986-41-4
(1R,2R,3S,4S)-3-(tert-Butyl-diphenyl-silanyloxy)-5-iodo-cyclohex-5-ene-1,2,4-triol

: 231934-87-5
(3aR,4R,5S,7aR)-4{[(1,1-dimethylethyl)diphenylsilyl]oxy}-3a,4,5,7a-tetrahydro-6-iodo-2,2-dimethyl-1,3-benzodioxol-5-ol

Guidance literature:: With toluene-4-sulfonic acid; at 18 ℃; for 3h;
DOI:10.1039/b106419c

Reference yield:

: 58479-61-1
tert-butylchlorodiphenylsilane

: 231934-87-5
(3aR,4R,5S,7aR)-4{[(1,1-dimethylethyl)diphenylsilyl]oxy}-3a,4,5,7a-tetrahydro-6-iodo-2,2-dimethyl-1,3-benzodioxol-5-ol

Guidance literature:: Multi-step reaction with 3 steps

1: 97 percent / imidazole / CH₂Cl₂ / 7 h / 18 °C

2: 98 percent / osmium tetroxide; N-methylmorpholine-N-oxide / 2-methyl-propan-2-ol; acetone; H₂O / 30 h / 4 °C

3: 85 percent / p-TsOH / 3 h / 18 °C

With 1H-imidazole; osmium(VIII) oxide; toluene-4-sulfonic acid; 4-methylmorpholine N-oxide; In dichloromethane; water; acetone; tert-butyl alcohol;
DOI:10.1039/b106419c

Reference yield:

: 300830-78-8
(1S,6S)-6-{[(1,1-dimethylethyl)diphenylsilyl]oxy}-2-iodocyclohexa-2,4-dien-1-ol

: 231934-87-5
(3aR,4R,5S,7aR)-4{[(1,1-dimethylethyl)diphenylsilyl]oxy}-3a,4,5,7a-tetrahydro-6-iodo-2,2-dimethyl-1,3-benzodioxol-5-ol

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / osmium tetroxide; N-methylmorpholine-N-oxide / 2-methyl-propan-2-ol; acetone; H₂O / 30 h / 4 °C

2: 85 percent / p-TsOH / 3 h / 18 °C

With osmium(VIII) oxide; toluene-4-sulfonic acid; 4-methylmorpholine N-oxide; In water; acetone; tert-butyl alcohol;
DOI:10.1039/b106419c