tert-butyl 7-benzyloxycarbonyl-7-azabicyclo<2.2.1>-2-heptene-1-carboxylate

Base Information

Chemical Name:tert-butyl 7-benzyloxycarbonyl-7-azabicyclo<2.2.1>-2-heptene-1-carboxylate
CAS No.:221677-07-2
Molecular Formula:C₁₉H₂₃NO₄
Molecular Weight:329.396
Hs Code.:

Synonyms:tert-butyl 7-benzyloxycarbonyl-7-azabicyclo<2.2.1>-2-heptene-1-carboxylate

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Chemical Property of tert-butyl 7-benzyloxycarbonyl-7-azabicyclo<2.2.1>-2-heptene-1-carboxylate

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Technology Process of tert-butyl 7-benzyloxycarbonyl-7-azabicyclo<2.2.1>-2-heptene-1-carboxylate

There total 2 articles about tert-butyl 7-benzyloxycarbonyl-7-azabicyclo<2.2.1>-2-heptene-1-carboxylate 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: 77.0%

: 221677-06-1
(2R,3S,5S)-3-tert-butyldimethylsilyloxy-1-benzyloxycarbonyl-5-β-bromoethylproline tert-butyl ester

: 221677-07-2
tert-butyl 7-benzyloxycarbonyl-7-azabicyclo<2.2.1>-2-heptene-1-carboxylate

Guidance literature:: With potassium hexamethylsilazane; In tetrahydrofuran; toluene; 1.) -78 deg C, 1 h, 2.) -40 deg C, 2 h, then 0 deg C, 1 h;
DOI:10.1021/jo982327c

Reference yield:

: C₁₅H₁₅NO₄

: 36805-97-7
N,N-dimethylformamide di-tert-butyl acetal

: 221677-07-2
tert-butyl 7-benzyloxycarbonyl-7-azabicyclo<2.2.1>-2-heptene-1-carboxylate

Guidance literature:: In toluene; for 1h; Reflux;
DOI:10.1055/s-0030-1257907

Reference yield: 88.0%

: 221677-07-2
tert-butyl 7-benzyloxycarbonyl-7-azabicyclo<2.2.1>-2-heptene-1-carboxylate

: 221677-08-3
tert-butyl (1S,2S,3R,4R)-7-benzyloxycarbonyl-2,3-dihydroxy-7-azabicyclo<2.2.1>heptane-1-carboxylate

Guidance literature:: With osmium(VIII) oxide; 4-methylmorpholine N-oxide; In water; acetone; for 12h; Ambient temperature;
DOI:10.1021/jo982327c