(3S,4R,5S)-3,4-Bis-benzyloxy-5-((S)-3-hydroxy-1-methoxymethoxy-propyl)-pyrrolidin-2-one

Base Information

Chemical Name:(3S,4R,5S)-3,4-Bis-benzyloxy-5-((S)-3-hydroxy-1-methoxymethoxy-propyl)-pyrrolidin-2-one
CAS No.:1054655-54-7
Molecular Formula:C₂₃H₂₉NO₆
Molecular Weight:415.486
Hs Code.:

Synonyms:(3S,4R,5S)-3,4-Bis-benzyloxy-5-((S)-3-hydroxy-1-methoxymethoxy-propyl)-pyrrolidin-2-one

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Chemical Property of (3S,4R,5S)-3,4-Bis-benzyloxy-5-((S)-3-hydroxy-1-methoxymethoxy-propyl)-pyrrolidin-2-one

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Technology Process of (3S,4R,5S)-3,4-Bis-benzyloxy-5-((S)-3-hydroxy-1-methoxymethoxy-propyl)-pyrrolidin-2-one

There total 11 articles about (3S,4R,5S)-3,4-Bis-benzyloxy-5-((S)-3-hydroxy-1-methoxymethoxy-propyl)-pyrrolidin-2-one 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:

: 312515-17-6
(S)-3-((2S,3R,4S)-3,4-Bis-benzyloxy-5-oxo-pyrrolidin-2-yl)-3-methoxymethoxy-propionaldehyde

: 1054655-54-7
(3S,4R,5S)-3,4-Bis-benzyloxy-5-((S)-3-hydroxy-1-methoxymethoxy-propyl)-pyrrolidin-2-one

Guidance literature:: With sodium tetrahydroborate; In ethanol;
DOI:10.1016/S0040-4039(00)01314-9

Reference yield:

: 160549-10-0
2,3,5-tri-O-benzyl-D-arabinofuranose

: 1054655-54-7
(3S,4R,5S)-3,4-Bis-benzyloxy-5-((S)-3-hydroxy-1-methoxymethoxy-propyl)-pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 11 steps

1: 100 percent / MS 4 Angstroem / benzene; CHCl₃ / reflux

2: 70 percent / tetrahydrofuran / -78 - -40 °C

3: 68 percent / PCC; MS 4 Angstroem / CH₂Cl₂

4: 98 percent / OsO₄; NMO / acetone; H₂O

5: NaIO₄ / diethyl ether; H₂O

6: BF₃*Et₂O / CH₂Cl₂ / -78 - -20 °C

7: 71 percent / CAN / acetonitrile; H₂O

8: 75 percent / (i-Pr)2NEt / CH₂Cl₂

9: 91 percent / OsO₄; NMO / acetone; H₂O

10: NaIO₄ / diethyl ether; H₂O

11: NaBH₄ / ethanol

With sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; N-methyl-2-indolinone; ammonium cerium(IV) nitrate; MS 4 Angstroem; boron trifluoride diethyl etherate; N-ethyl-N,N-diisopropylamine; pyridinium chlorochromate; In tetrahydrofuran; diethyl ether; ethanol; dichloromethane; chloroform; water; acetone; acetonitrile; benzene; 1: Condensation / 2: Addition / 3: Oxidation / 4: Oxidation / 5: Oxidation / 6: Addition / 7: Oxidation / 8: Etherification / 9: Oxidation / 10: Oxidation / 11: Reduction;
DOI:10.1016/S0040-4039(00)01314-9

Reference yield:

: 157831-26-0
(3S,4R,5S)-3,4-dibenzyloxy-1-(4-methoxyphenylmethyl)-5-vinylpyrrolidin-2-one

: 1054655-54-7
(3S,4R,5S)-3,4-Bis-benzyloxy-5-((S)-3-hydroxy-1-methoxymethoxy-propyl)-pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 8 steps

1: 98 percent / OsO₄; NMO / acetone; H₂O

2: NaIO₄ / diethyl ether; H₂O

3: BF₃*Et₂O / CH₂Cl₂ / -78 - -20 °C

4: 71 percent / CAN / acetonitrile; H₂O

5: 75 percent / (i-Pr)2NEt / CH₂Cl₂

6: 91 percent / OsO₄; NMO / acetone; H₂O

7: NaIO₄ / diethyl ether; H₂O

8: NaBH₄ / ethanol

With sodium tetrahydroborate; sodium periodate; osmium(VIII) oxide; N-methyl-2-indolinone; ammonium cerium(IV) nitrate; boron trifluoride diethyl etherate; N-ethyl-N,N-diisopropylamine; In diethyl ether; ethanol; dichloromethane; water; acetone; acetonitrile; 1: Oxidation / 2: Oxidation / 3: Addition / 4: Oxidation / 5: Etherification / 6: Oxidation / 7: Oxidation / 8: Reduction;
DOI:10.1016/S0040-4039(00)01314-9