(1R,4R,5S,6S,7S)-4-exo<(benzyloxy)methyl>-6-exo,7-exo-(isopropylidenedioxy)-4-endo-methyl-2,8-dioxabicyclo<3.2.1>octan-3-one

Base Information

Chemical Name:(1R,4R,5S,6S,7S)-4-exo<(benzyloxy)methyl>-6-exo,7-exo-(isopropylidenedioxy)-4-endo-methyl-2,8-dioxabicyclo<3.2.1>octan-3-one
CAS No.:136171-89-6
Molecular Formula:C₁₈H₂₂O₆
Molecular Weight:334.369
Hs Code.:

Synonyms:(1R,4R,5S,6S,7S)-4-exo<(benzyloxy)methyl>-6-exo,7-exo-(isopropylidenedioxy)-4-endo-methyl-2,8-dioxabicyclo<3.2.1>octan-3-one

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (1R,4R,5S,6S,7S)-4-exo<(benzyloxy)methyl>-6-exo,7-exo-(isopropylidenedioxy)-4-endo-methyl-2,8-dioxabicyclo<3.2.1>octan-3-one

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Technology Process of (1R,4R,5S,6S,7S)-4-exo<(benzyloxy)methyl>-6-exo,7-exo-(isopropylidenedioxy)-4-endo-methyl-2,8-dioxabicyclo<3.2.1>octan-3-one

There total 4 articles about (1R,4R,5S,6S,7S)-4-exo<(benzyloxy)methyl>-6-exo,7-exo-(isopropylidenedioxy)-4-endo-methyl-2,8-dioxabicyclo<3.2.1>octan-3-one 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:

: 17690-16-3
benzyl bromomethyl ether

: 127588-86-7,127588-88-9,136029-21-5,139578-28-2
(1RS,4RS,5SR,6SR,7SR)-6-exo,7-exo-(isopropylidenedioxy)-4-exo-methyl-2,8-dioxabicyclo<3.2.1>octan-3-one

: 127588-90-3,136171-89-6
(1RS,4RS,5SR,6SR,7SR)-4-exo<(benzyloxy)methyl>-6-exo,7-exo-(isopropylidenedioxy)-4-endo-methyl-2,8-dioxabicyclo<3.2.1>octan-3-one

Guidance literature:: With lithium hexamethyldisilazane; Multistep reaction; 1) hexane, THF, -60 deg C, 2 h, 2) up to -10 deg C, 30 min;
DOI:10.1016/S0040-4020(01)91030-0

Reference yield:

: 84121-01-7,118244-89-6,118244-90-9
6-exo,7-exo-(isopropylidenedioxy)-2,8-dioxabicyclo<3.2.1>octan-3-one

: 127588-90-3,136171-89-6
(1RS,4RS,5SR,6SR,7SR)-4-exo<(benzyloxy)methyl>-6-exo,7-exo-(isopropylidenedioxy)-4-endo-methyl-2,8-dioxabicyclo<3.2.1>octan-3-one

Guidance literature:: Multi-step reaction with 2 steps

1: 98 percent / (Me₃Si)2NLi / tetrahydrofuran / -65 - -20 °C

2: (Me₃Si)2NLi / tetrahydrofuran / -60 - -10 °C

With lithium hexamethyldisilazane; In tetrahydrofuran;
DOI:10.1039/c39890001634

Reference yield:

: 17690-16-3
benzyl bromomethyl ether

: 136029-21-5
(1S,2S,6S,7R,10R)-4,4,10-Trimethyl-3,5,8,11-tetraoxa-tricyclo[5.3.1.0^2,6]undecan-9-one

: 136171-89-6
(1R,4R,5S,6S,7S)-4-exo<(benzyloxy)methyl>-6-exo,7-exo-(isopropylidenedioxy)-4-endo-methyl-2,8-dioxabicyclo<3.2.1>octan-3-one

Guidance literature:: With lithium hexamethyldisilazane; Yield given. Multistep reaction; 1) THF, -60 deg C 2) -60 to -10 deg C, 30 min;
DOI:10.1016/S0040-4039(00)79713-9