methyl (1R,2S,3R,4S)-3-[(4-fluorobenzyl)amino]-7-oxabicyclo[2.2.1]heptane-2-carboxylate

Base Information

Chemical Name:methyl (1R,2S,3R,4S)-3-[(4-fluorobenzyl)amino]-7-oxabicyclo[2.2.1]heptane-2-carboxylate
CAS No.:1071521-02-2
Molecular Formula:C₁₅H₁₈FNO₃
Molecular Weight:279.311
Hs Code.:

Synonyms:methyl (1R,2S,3R,4S)-3-[(4-fluorobenzyl)amino]-7-oxabicyclo[2.2.1]heptane-2-carboxylate

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Chemical Property of methyl (1R,2S,3R,4S)-3-[(4-fluorobenzyl)amino]-7-oxabicyclo[2.2.1]heptane-2-carboxylate

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Technology Process of methyl (1R,2S,3R,4S)-3-[(4-fluorobenzyl)amino]-7-oxabicyclo[2.2.1]heptane-2-carboxylate

There total 10 articles about methyl (1R,2S,3R,4S)-3-[(4-fluorobenzyl)amino]-7-oxabicyclo[2.2.1]heptane-2-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:

: 1071521-05-5
methyl (1R,2S,3R,4S)-3-(4-fluorobenzylamino)-7-oxabicyclo[2.2.1]heptane-2-carboxylate mandelic acid salt

: 1071521-02-2
methyl (1R,2S,3R,4S)-3-[(4-fluorobenzyl)amino]-7-oxabicyclo[2.2.1]heptane-2-carboxylate

Guidance literature:: With sodium hydrogencarbonate; In water; ethyl acetate; at 25 ℃; for 0.5h;

Reference yield:

: 1071520-82-5
methyl (1R,2S,3R,4S)-3-amino-7-oxabicyclo[2.2.1]heptane-2-carboxylate

: 459-57-4
4-fluorobenzaldehyde

: 1071521-02-2
methyl (1R,2S,3R,4S)-3-[(4-fluorobenzyl)amino]-7-oxabicyclo[2.2.1]heptane-2-carboxylate

: methyl (1S,2R,3S,4R)-3-[(4-fluorobenzyl)amino]-7-oxabicyclo[2.2.1]heptane-2-carboxylate

Guidance literature:: methyl (1R,2S,3R,4S)-3-amino-7-oxabicyclo[2.2.1]heptane-2-carboxylate; 4-fluorobenzaldehyde; In methanol; at 25 ℃; for 0.166667h;

With sodium cyanoborohydride; acetic acid; In methanol; at 25 ℃; for 18h;

Reference yield:

: 1071520-79-0
methyl (1R,2S,3R,4S)-3-{[(benzyloxy)carbonyl]amino}-7-oxabicyclo[2.2.1]heptane-2-carboxylate

: 1071521-02-2
methyl (1R,2S,3R,4S)-3-[(4-fluorobenzyl)amino]-7-oxabicyclo[2.2.1]heptane-2-carboxylate

: methyl (1S,2R,3S,4R)-3-[(4-fluorobenzyl)amino]-7-oxabicyclo[2.2.1]heptane-2-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1.1: hydrogen / 5%-palladium/activated carbon / ethyl acetate / 16 h / 20 °C

2.1: methanol / 0.17 h / 25 °C

2.2: 18 h / 25 °C

With hydrogen; 5%-palladium/activated carbon; In methanol; ethyl acetate;