(7R,7aR)-7-(2-Nitro-benzyloxy)-5,6,7,7a-tetrahydro-3H-pyrrolizine-1-carboxylic acid methyl ester

Base Information

Chemical Name:(7R,7aR)-7-(2-Nitro-benzyloxy)-5,6,7,7a-tetrahydro-3H-pyrrolizine-1-carboxylic acid methyl ester
CAS No.:96246-62-7
Molecular Formula:C₁₆H₁₈N₂O₅
Molecular Weight:318.329
Hs Code.:

Synonyms:(7R,7aR)-7-(2-Nitro-benzyloxy)-5,6,7,7a-tetrahydro-3H-pyrrolizine-1-carboxylic acid methyl ester

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Chemical Property of (7R,7aR)-7-(2-Nitro-benzyloxy)-5,6,7,7a-tetrahydro-3H-pyrrolizine-1-carboxylic acid methyl ester

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Technology Process of (7R,7aR)-7-(2-Nitro-benzyloxy)-5,6,7,7a-tetrahydro-3H-pyrrolizine-1-carboxylic acid methyl ester

There total 1 articles about (7R,7aR)-7-(2-Nitro-benzyloxy)-5,6,7,7a-tetrahydro-3H-pyrrolizine-1-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:

: 96246-61-6
(7R,7aS)-7-(2-Nitro-benzyloxy)-1-phenylselanyl-hexahydro-pyrrolizine-1-carboxylic acid methyl ester

: 96246-63-8
7-(2-Nitro-benzyloxy)-6,7-dihydro-5H-pyrrolizine-1-carboxylic acid methyl ester

: 96246-62-7
(7R,7aR)-7-(2-Nitro-benzyloxy)-5,6,7,7a-tetrahydro-3H-pyrrolizine-1-carboxylic acid methyl ester

Guidance literature:: With dimethylsulfide; 3-chloro-benzenecarboperoxoic acid; Yield given. Multistep reaction. Yields of byproduct given; 1.) methylene chloride, - 78 deg C, 2 h 2.) 1 h;
DOI:10.1021/jo00212a034

Reference yield: 100.0%

: 96246-62-7
(7R,7aR)-7-(2-Nitro-benzyloxy)-5,6,7,7a-tetrahydro-3H-pyrrolizine-1-carboxylic acid methyl ester

: 96246-64-9
[(7R,7aR)-7-(2-Nitro-benzyloxy)-5,6,7,7a-tetrahydro-3H-pyrrolizin-1-yl]-methanol

Guidance literature:: With diisobutylaluminium hydride; In hexane; dichloromethane; at -23 ℃; for 1h;
DOI:10.1021/jo00212a034

Reference yield:

: 96246-62-7
(7R,7aR)-7-(2-Nitro-benzyloxy)-5,6,7,7a-tetrahydro-3H-pyrrolizine-1-carboxylic acid methyl ester

: 96246-65-0
(2S,3R)-2,3-Dihydroxy-2-isopropyl-butyric acid (7S,7aS)-7-(2-nitro-benzyloxy)-5,6,7,7a-tetrahydro-3H-pyrrolizin-1-ylmethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 100 percent / diisobutylaluminum hydride / CH₂Cl₂; hexane / 1 h / -23 °C

2: N,N'-dicyclohexylcarbodiimide, (N,N-dimethylamino)pyridine / toluene / 14 h

With dmap; diisobutylaluminium hydride; dicyclohexyl-carbodiimide; In hexane; dichloromethane; toluene;
DOI:10.1021/jo00212a034