2-[(2S,3S,3aR,5R,6aR)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-hexahydro-furo[2,3-b]furan-3-yl]-ethanol

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Chemical Name:2-[(2S,3S,3aR,5R,6aR)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-hexahydro-furo[2,3-b]furan-3-yl]-ethanol
CAS No.:876173-61-4
Molecular Formula:C₂₆H₃₆O₅Si
Molecular Weight:456.654
Hs Code.:

Synonyms:2-[(2S,3S,3aR,5R,6aR)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-hexahydro-furo[2,3-b]furan-3-yl]-ethanol

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Chemical Property of 2-[(2S,3S,3aR,5R,6aR)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-hexahydro-furo[2,3-b]furan-3-yl]-ethanol

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Technology Process of 2-[(2S,3S,3aR,5R,6aR)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-hexahydro-furo[2,3-b]furan-3-yl]-ethanol

There total 7 articles about 2-[(2S,3S,3aR,5R,6aR)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-hexahydro-furo[2,3-b]furan-3-yl]-ethanol 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:

: 678160-07-1
[(2S,3S,3aR,5R,6aR)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-hexahydro-furo[2,3-b]furan-3-yl]-acetaldehyde

: 876173-61-4
2-[(2S,3S,3aR,5R,6aR)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-hexahydro-furo[2,3-b]furan-3-yl]-ethanol

Guidance literature:: With sodium tetrahydroborate; In methanol; at 25 ℃; for 0.5h;
DOI:10.1002/anie.200352868

Reference yield:

: 99315-76-1
(5S)-5-(tert-butyldiphenylsiloxymethyl)-2(5H)-furanone

: 876173-61-4
2-[(2S,3S,3aR,5R,6aR)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-hexahydro-furo[2,3-b]furan-3-yl]-ethanol

Guidance literature:: Multi-step reaction with 6 steps

1: 85 percent / AlCl₃ / CH₂Cl₂ / 144 h / 60 °C

2: 98 percent / DIBAL-H / CH₂Cl₂; toluene / 0.5 h / -78 °C

3: aq. OsO₄; NMO / acetone; 2-methyl-propan-2-ol / 10 h / 25 °C

4: 8.9 g / Pb(OAc)4 / CH₂Cl₂ / 0.25 h / 0 °C

5: 38.5 percent / Amberlyst 15; 3 Angstroem molecular sieves / diethyl ether / 10 h / 25 °C

6: NaBH₄ / methanol / 25 °C

With lead(IV) acetate; sodium tetrahydroborate; osmium(VIII) oxide; aluminium trichloride; N-methyl-2-indolinone; Amberlyst 15; 3 A molecular sieve; diisobutylaluminium hydride; In methanol; diethyl ether; dichloromethane; acetone; toluene; tert-butyl alcohol; 1: Diels-Alder reaction;
DOI:10.1002/chem.200500513

Reference yield:

: 99333-00-3
(+)-(1R,6S,7S)-7-diphenyl-t-butylsiloxymethyl-8-oxabicyclo-<4.3.0>non-3-en-9-one

: 876173-61-4
2-[(2S,3S,3aR,5R,6aR)-2-(tert-Butyl-diphenyl-silanyloxymethyl)-5-methoxy-hexahydro-furo[2,3-b]furan-3-yl]-ethanol

Guidance literature:: Multi-step reaction with 5 steps

1: 98 percent / DIBAL-H / CH₂Cl₂; toluene / 0.5 h / -78 °C

2: aq. OsO₄; NMO / acetone; 2-methyl-propan-2-ol / 10 h / 25 °C

3: 8.9 g / Pb(OAc)4 / CH₂Cl₂ / 0.25 h / 0 °C

4: 38.5 percent / Amberlyst 15; 3 Angstroem molecular sieves / diethyl ether / 10 h / 25 °C

5: NaBH₄ / methanol / 25 °C

With lead(IV) acetate; sodium tetrahydroborate; osmium(VIII) oxide; N-methyl-2-indolinone; Amberlyst 15; 3 A molecular sieve; diisobutylaluminium hydride; In methanol; diethyl ether; dichloromethane; acetone; toluene; tert-butyl alcohol;
DOI:10.1002/chem.200500513