(1S,5S,7R)-3-(tert-butoxycarbonyl)-5-phenyl-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid methyl ester

Base Information

Chemical Name:(1S,5S,7R)-3-(tert-butoxycarbonyl)-5-phenyl-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid methyl ester
CAS No.:515821-72-4
Molecular Formula:C₁₈H₂₃NO₆
Molecular Weight:349.384
Hs Code.:

Synonyms:(1S,5S,7R)-3-(tert-butoxycarbonyl)-5-phenyl-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid methyl ester

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Chemical Property of (1S,5S,7R)-3-(tert-butoxycarbonyl)-5-phenyl-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid methyl ester

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Technology Process of (1S,5S,7R)-3-(tert-butoxycarbonyl)-5-phenyl-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid methyl ester

There total 4 articles about (1S,5S,7R)-3-(tert-butoxycarbonyl)-5-phenyl-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-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: 94.0%

: 24424-99-5
di-tert-butyl dicarbonate

: 515821-71-3
(1S,5S,7R)-3-benzhydryl-5-phenyl-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid methyl ester

: 515821-72-4
(1S,5S,7R)-3-(tert-butoxycarbonyl)-5-phenyl-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid methyl ester

Guidance literature:: With ammonium formate; palladium on activated charcoal; In methanol; for 1h; Heating;
DOI:10.1016/S0040-4020(02)01297-8

Reference yield:

: 23934-75-0
2-(benzhydrylamino)-1-phenyl-1-ethanone

: 515821-72-4
(1S,5S,7R)-3-(tert-butoxycarbonyl)-5-phenyl-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 4 steps

1.1: CH₂Cl₂ / 0 - 30 °C

2.1: thionyl chloride / 2 h / 60 °C

2.2: 65.0 g / TFA / CH₂Cl₂ / 3 h / -10 °C

3.1: 70 percent / BH₃*Me₂S / tetrahydrofuran / 0 - 20 °C

4.1: 94 percent / ammonium formate / 10 percent Pd/C / methanol / 1 h / Heating

With thionyl chloride; dimethylsulfide borane complex; ammonium formate; palladium on activated charcoal; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1016/S0040-4020(02)01297-8

Reference yield:

: 515821-69-9
(1R,5S,7R)-3-benzhydryl-2-oxo-5-phenyl-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid methyl ester

: 515821-72-4
(1S,5S,7R)-3-(tert-butoxycarbonyl)-5-phenyl-6,8-dioxa-3-azabicyclo[3.2.1]octane-7-carboxylic acid methyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / BH₃*Me₂S / tetrahydrofuran / 0 - 20 °C

2: 94 percent / ammonium formate / 10 percent Pd/C / methanol / 1 h / Heating

With dimethylsulfide borane complex; ammonium formate; palladium on activated charcoal; In tetrahydrofuran; methanol;
DOI:10.1016/S0040-4020(02)01297-8