phenyl (1S,3R)-1-azidoacetoxy-3-methoxymethyl-2,2,3-trimethylcyclopentane-1-carboxylate

Base Information

Chemical Name:phenyl (1S,3R)-1-azidoacetoxy-3-methoxymethyl-2,2,3-trimethylcyclopentane-1-carboxylate
CAS No.:244233-16-7
Molecular Formula:C₁₉H₂₅N₃O₅
Molecular Weight:375.425
Hs Code.:

Synonyms:phenyl (1S,3R)-1-azidoacetoxy-3-methoxymethyl-2,2,3-trimethylcyclopentane-1-carboxylate

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Chemical Property of phenyl (1S,3R)-1-azidoacetoxy-3-methoxymethyl-2,2,3-trimethylcyclopentane-1-carboxylate

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Technology Process of phenyl (1S,3R)-1-azidoacetoxy-3-methoxymethyl-2,2,3-trimethylcyclopentane-1-carboxylate

There total 4 articles about phenyl (1S,3R)-1-azidoacetoxy-3-methoxymethyl-2,2,3-trimethylcyclopentane-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: 93.0%

: 244233-14-5
phenyl (1S,3R)-1-chloracetoxy-3-methoxymethyl-2,2,3-trimethylcyclopentane-1-carboxylate

: 244233-16-7
phenyl (1S,3R)-1-azidoacetoxy-3-methoxymethyl-2,2,3-trimethylcyclopentane-1-carboxylate

Guidance literature:: With sodium azide; In acetonitrile; at 70 - 75 ℃; for 7h;
DOI:10.1002/(SICI)1099-0690(199908)1999:8<1967::AID-EJOC1967>3.0.CO;2-G

Reference yield:

: 120697-88-3
(1S,3R)-1-hydroxy-3-methoxymethyl-2,2,3-trimethylcyclopentane-1-carboxylic acid

: 244233-16-7
phenyl (1S,3R)-1-azidoacetoxy-3-methoxymethyl-2,2,3-trimethylcyclopentane-1-carboxylate

Guidance literature:: Multi-step reaction with 4 steps

1: tetrahydrofuran / 16 h / 20 °C

2: tetrahydrofuran / 7 h / Heating

3: 96 percent / 24 h / 20 °C

4: 93 percent / NaN₃ / acetonitrile / 7 h / 70 - 75 °C

With sodium azide; In tetrahydrofuran; acetonitrile; 1: Acylation / 2: Esterification / 3: Acylation / 4: Substitution;
DOI:10.1002/(SICI)1099-0690(199908)1999:8<1967::AID-EJOC1967>3.0.CO;2-G

Reference yield:

: 244233-12-3
phenyl (1S,3R)-1-hydroxy-3-methoxymethyl-2,2,3-trimethylcyclopentane-1-carboxylate

: 244233-16-7
phenyl (1S,3R)-1-azidoacetoxy-3-methoxymethyl-2,2,3-trimethylcyclopentane-1-carboxylate

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / 24 h / 20 °C

2: 93 percent / NaN₃ / acetonitrile / 7 h / 70 - 75 °C

With sodium azide; In acetonitrile; 1: Acylation / 2: Substitution;
DOI:10.1002/(SICI)1099-0690(199908)1999:8<1967::AID-EJOC1967>3.0.CO;2-G