(2R,3R,4aS,8R,8aS)-8-Amino-3-benzyloxy-2-benzyloxymethyl-octahydro-chromene-8-carboxylic acid methyl ester

Base Information

Chemical Name:(2R,3R,4aS,8R,8aS)-8-Amino-3-benzyloxy-2-benzyloxymethyl-octahydro-chromene-8-carboxylic acid methyl ester
CAS No.:1054659-34-5
Molecular Formula:C₂₆H₃₃NO₅
Molecular Weight:439.552
Hs Code.:

Synonyms:(2R,3R,4aS,8R,8aS)-8-Amino-3-benzyloxy-2-benzyloxymethyl-octahydro-chromene-8-carboxylic acid methyl ester

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Chemical Property of (2R,3R,4aS,8R,8aS)-8-Amino-3-benzyloxy-2-benzyloxymethyl-octahydro-chromene-8-carboxylic acid methyl ester

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Technology Process of (2R,3R,4aS,8R,8aS)-8-Amino-3-benzyloxy-2-benzyloxymethyl-octahydro-chromene-8-carboxylic acid methyl ester

There total 4 articles about (2R,3R,4aS,8R,8aS)-8-Amino-3-benzyloxy-2-benzyloxymethyl-octahydro-chromene-8-carboxylic acid methyl 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:

: 871695-72-6
(2R,3R,8R,8aS)-3-Benzyloxy-2-benzyloxymethyl-8-nitro-3,4,6,7,8,8a-hexahydro-2H-chromene-8-carboxylic acid methyl ester

: 1054659-34-5
(2R,3R,4aS,8R,8aS)-8-Amino-3-benzyloxy-2-benzyloxymethyl-octahydro-chromene-8-carboxylic acid methyl ester

Guidance literature:: With platinized Raney Ni (T₄); hydrogen; In ethanol; at 20 ℃; for 2h;
DOI:10.1021/ol052190u

Reference yield:

: 871695-96-4
1,5-anhydro-4,6-di-O-benzyl-2,3-dideoxy-2-C-formyl-D-threohex-1-enitol

: 1054659-34-5
(2R,3R,4aS,8R,8aS)-8-Amino-3-benzyloxy-2-benzyloxymethyl-octahydro-chromene-8-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 3 steps

1.1: n-BuLi / tetrahydrofuran / 0.5 h / 20 °C

1.2: 74 percent / tetrahydrofuran / 1 h / 20 °C

2.1: 71 percent / AcOH / tetrahydrofuran / 24 h / 35 - 40 °C

3.1: platinized Raney Ni (T₄); hydrogen / ethanol / 2 h / 20 °C

With n-butyllithium; platinized Raney Ni (T₄); hydrogen; acetic acid; In tetrahydrofuran; ethanol; 1.2: Wittig olefination / 2.1: Diels-Alder reaction;
DOI:10.1021/ol052190u

Reference yield:

: 871695-94-2
(2R,3R)-3-Benzyloxy-2-benzyloxymethyl-5-vinyl-3,4-dihydro-2H-pyran

: 1054659-34-5
(2R,3R,4aS,8R,8aS)-8-Amino-3-benzyloxy-2-benzyloxymethyl-octahydro-chromene-8-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 71 percent / AcOH / tetrahydrofuran / 24 h / 35 - 40 °C

2: platinized Raney Ni (T₄); hydrogen / ethanol / 2 h / 20 °C

With platinized Raney Ni (T₄); hydrogen; acetic acid; In tetrahydrofuran; ethanol; 1: Diels-Alder reaction;
DOI:10.1021/ol052190u