methyl (2R,3R)-(-)-N-benzyl-N-[(1R)-1-benzyloxymethyl-2-hydroxyethyl]-2,3-di-O-isopropylidenetartramate

Base Information

Chemical Name:methyl (2R,3R)-(-)-N-benzyl-N-[(1R)-1-benzyloxymethyl-2-hydroxyethyl]-2,3-di-O-isopropylidenetartramate
CAS No.:427882-48-2
Molecular Formula:C₂₅H₃₁NO₇
Molecular Weight:457.524
Hs Code.:

Synonyms:methyl (2R,3R)-(-)-N-benzyl-N-[(1R)-1-benzyloxymethyl-2-hydroxyethyl]-2,3-di-O-isopropylidenetartramate

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Chemical Property of methyl (2R,3R)-(-)-N-benzyl-N-[(1R)-1-benzyloxymethyl-2-hydroxyethyl]-2,3-di-O-isopropylidenetartramate

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Technology Process of methyl (2R,3R)-(-)-N-benzyl-N-[(1R)-1-benzyloxymethyl-2-hydroxyethyl]-2,3-di-O-isopropylidenetartramate

There total 4 articles about methyl (2R,3R)-(-)-N-benzyl-N-[(1R)-1-benzyloxymethyl-2-hydroxyethyl]-2,3-di-O-isopropylidenetartramate 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: 70.0%

: 67812-33-3
(4R,5R)-5-(methoxycarbonyl)-2,2-dimethyl-1,3-dioxolane-4-carboxylic acid

: 170956-48-6
(2R)-(+)-2-(N-benzylamino)-3-benzyloxy-1-propanol

: 427882-48-2
methyl (2R,3R)-(-)-N-benzyl-N-[(1R)-1-benzyloxymethyl-2-hydroxyethyl]-2,3-di-O-isopropylidenetartramate

Guidance literature:: With N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; In dichloromethane;
DOI:10.1002/1099-0690(200203)2002:5<873::AID-EJOC873>3.0.CO;2-V

Reference yield:

: 19525-87-2
O-methyl O-benzyl-L-serinate hydrochloride

: 427882-48-2
methyl (2R,3R)-(-)-N-benzyl-N-[(1R)-1-benzyloxymethyl-2-hydroxyethyl]-2,3-di-O-isopropylidenetartramate

Guidance literature:: Multi-step reaction with 3 steps

1: 5 percent / Et₃N / tetrahydrofuran / 15 h / 20 °C

2: 98 percent / LiAlH₄ / tetrahydrofuran

3: 70 percent / PyBrOP; DIPEA / CH₂Cl₂

With lithium aluminium tetrahydride; triethylamine; N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; In tetrahydrofuran; dichloromethane;
DOI:10.1002/1099-0690(200203)2002:5<873::AID-EJOC873>3.0.CO;2-V

Reference yield:

: 98-88-4
benzoyl chloride

: 427882-48-2
methyl (2R,3R)-(-)-N-benzyl-N-[(1R)-1-benzyloxymethyl-2-hydroxyethyl]-2,3-di-O-isopropylidenetartramate

Guidance literature:: Multi-step reaction with 3 steps

1: 5 percent / Et₃N / tetrahydrofuran / 15 h / 20 °C

2: 98 percent / LiAlH₄ / tetrahydrofuran

3: 70 percent / PyBrOP; DIPEA / CH₂Cl₂

With lithium aluminium tetrahydride; triethylamine; N-ethyl-N,N-diisopropylamine; bromo-tris(1-pyrrolidinyl)phosphonium hexafluorophosphate; In tetrahydrofuran; dichloromethane;
DOI:10.1002/1099-0690(200203)2002:5<873::AID-EJOC873>3.0.CO;2-V