Methanesulfonic acid (R)-1-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-3-[(2R,4R,6R)-6-methoxy-4-(4-methoxy-benzyloxy)-6-methyl-tetrahydro-pyran-2-yl]-propyl ester

Base Information

Chemical Name:Methanesulfonic acid (R)-1-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-3-[(2R,4R,6R)-6-methoxy-4-(4-methoxy-benzyloxy)-6-methyl-tetrahydro-pyran-2-yl]-propyl ester
CAS No.:322429-00-5
Molecular Formula:C₃₇H₅₂O₉SSi
Molecular Weight:700.966
Hs Code.:

Methanesulfonic acid (R)-1-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-3-[(2R,4R,6R)-6-methoxy-4-(4-methoxy-benzyloxy)-6-methyl-tetrahydro-pyran-2-yl]-propyl ester

Synonyms:Methanesulfonic acid (R)-1-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-3-[(2R,4R,6R)-6-methoxy-4-(4-methoxy-benzyloxy)-6-methyl-tetrahydro-pyran-2-yl]-propyl ester

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Chemical Property of Methanesulfonic acid (R)-1-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-3-[(2R,4R,6R)-6-methoxy-4-(4-methoxy-benzyloxy)-6-methyl-tetrahydro-pyran-2-yl]-propyl ester

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Technology Process of Methanesulfonic acid (R)-1-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-3-[(2R,4R,6R)-6-methoxy-4-(4-methoxy-benzyloxy)-6-methyl-tetrahydro-pyran-2-yl]-propyl ester

There total 8 articles about Methanesulfonic acid (R)-1-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-3-[(2R,4R,6R)-6-methoxy-4-(4-methoxy-benzyloxy)-6-methyl-tetrahydro-pyran-2-yl]-propyl ester 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:

: 322428-47-7
(4S)-5-[(4R,6R)-4-((E)-2-phenylethenyl)-2,2-dimethyl-1,3-dioxan-6-yl]-4-p-methoxybenzyloxy-2-pentene

: 322429-00-5
Methanesulfonic acid (R)-1-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-3-[(2R,4R,6R)-6-methoxy-4-(4-methoxy-benzyloxy)-6-methyl-tetrahydro-pyran-2-yl]-propyl ester

Guidance literature:: Multi-step reaction with 9 steps

1.1: 77 percent / O₂; PdCl₂; Cu(OAc)2*H₂O / N,N-dimethyl-acetamide; H₂O / 19.5 h / 20 °C

2.1: 85 percent / PPTS / methanol / 6.5 h

3.1: NaH / tetrahydrofuran / 0.5 h / 0 °C

3.2: 98 percent / tetrahydrofuran / 14.67 h / 0 - 20 °C

4.1: OsO₄; NMO / acetone; H₂O; 2-methyl-propan-2-ol / 5 h / 20 °C

5.1: NaIO₄; sodium phosphate / tetrahydrofuran; H₂O / 0.42 h / 0 - 20 °C / pH 7

6.1: 134 mg / tetrahydrofuran; toluene / 0.2 h / -78 - 0 °C

7.1: 83 mg / OsO₄; NMO / acetone; H₂O; 2-methyl-propan-2-ol / 4.5 h / 20 °C

8.1: 129 mg / Et₃N; DMAP / CH₂Cl₂ / 13.83 h / 0 - 20 °C

9.1: Et₃N; DMAP / CH₂Cl₂ / 2.25 h / 0 - 20 °C

With dmap; sodium periodate; osmium(VIII) oxide; N-methyl-2-indolinone; copper diacetate; oxygen; pyridinium p-toluenesulfonate; sodium hydride; triethylamine; sodium phosphate; palladium dichloride; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl acetamide; water; acetone; toluene; tert-butyl alcohol; 1.1: Wacker oxidation / 6.1: Tebbe olefination;
DOI:10.1016/S0040-4020(01)00593-2

Reference yield:

: 124-63-0
methanesulfonyl chloride

: 322428-57-9
(3R)-4-[(2R,4R,6R)-4-p-methoxybenzyloxy-2-methoxy-2-methyltetrahydropyran-6-yl]-3-methoxy-1-tert-butyldiphenylsiloxy-2-butanol

: 322429-00-5
Methanesulfonic acid (R)-1-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-3-[(2R,4R,6R)-6-methoxy-4-(4-methoxy-benzyloxy)-6-methyl-tetrahydro-pyran-2-yl]-propyl ester

Guidance literature:: With dmap; triethylamine; In dichloromethane; at 0 - 20 ℃; for 2.25h;
DOI:10.1016/S0040-4020(01)00593-2

Reference yield:

: 322428-96-6
(R)-2-Methoxy-3-[(2R,4R,6R)-6-methoxy-4-(4-methoxy-benzyloxy)-6-methyl-tetrahydro-pyran-2-yl]-propionaldehyde

: 322429-00-5
Methanesulfonic acid (R)-1-(tert-butyl-diphenyl-silanyloxymethyl)-2-methoxy-3-[(2R,4R,6R)-6-methoxy-4-(4-methoxy-benzyloxy)-6-methyl-tetrahydro-pyran-2-yl]-propyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: 134 mg / tetrahydrofuran; toluene / 0.2 h / -78 - 0 °C

2: 83 mg / OsO₄; NMO / acetone; H₂O; 2-methyl-propan-2-ol / 4.5 h / 20 °C

3: 129 mg / Et₃N; DMAP / CH₂Cl₂ / 13.83 h / 0 - 20 °C

4: Et₃N; DMAP / CH₂Cl₂ / 2.25 h / 0 - 20 °C

With dmap; osmium(VIII) oxide; N-methyl-2-indolinone; triethylamine; In tetrahydrofuran; dichloromethane; water; acetone; toluene; tert-butyl alcohol; 1: Tebbe olefination;
DOI:10.1016/S0040-4020(01)00593-2