N-<4-(Benzyloxy)-3-(formyloxy)phenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide

Base Information

• Chemical Name: N-<4-(Benzyloxy)-3-(formyloxy)phenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide
• CAS No.: 1027958-99-1
• Molecular Formula: C₂₃H₂₅NO₆
• Molecular Weight: 411.455
• Mol file: 1027958-99-1.mol

Synonyms:N-<4-(Benzyloxy)-3-(formyloxy)phenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide

Chemical Property of N-<4-(Benzyloxy)-3-(formyloxy)phenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of N-<4-(Benzyloxy)-3-(formyloxy)phenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide

There total 3 articles about N-<4-(Benzyloxy)-3-(formyloxy)phenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide 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%

N-<4-(Benzyloxy)-3-formylphenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide (151513-24-5) → N-<4-(Benzyloxy)-3-(formyloxy)phenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide (1027958-99-1)

Guidance literature:

With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; for 14h; Ambient temperature;

DOI:10.1021/jo00078a046

Reference yield:

N-<4-(benzyloxy)-3-(benzyloxycarbonyl)phenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide (144019-62-5) → N-<4-(Benzyloxy)-3-(formyloxy)phenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide (1027958-99-1)

Guidance literature:

Multi-step reaction with 3 steps

1: 93 percent / LiAlH₄ / tetrahydrofuran / 0.5 h / 0 °C

2: 87 percent / PCC, molecular sieves 4 Angstroem / CH₂Cl₂ / 1 h / Ambient temperature

3: 77 percent / mCPBA / CH₂Cl₂ / 14 h / Ambient temperature

With lithium aluminium tetrahydride; 4 A molecular sieve; 3-chloro-benzenecarboperoxoic acid; pyridinium chlorochromate; In tetrahydrofuran; dichloromethane;

DOI:10.1021/jo00078a046

Reference yield:

N-<4-(Benzyloxy)-3-(hydroxymethyl)phenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide (151513-23-4) → N-<4-(Benzyloxy)-3-(formyloxy)phenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide (1027958-99-1)

Guidance literature:

Multi-step reaction with 2 steps

1: 87 percent / PCC, molecular sieves 4 Angstroem / CH₂Cl₂ / 1 h / Ambient temperature

2: 77 percent / mCPBA / CH₂Cl₂ / 14 h / Ambient temperature

With 4 A molecular sieve; 3-chloro-benzenecarboperoxoic acid; pyridinium chlorochromate; In dichloromethane;

DOI:10.1021/jo00078a046

upstream raw materials:

N-<4-(Benzyloxy)-3-formylphenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide

N-<4-(benzyloxy)-3-(benzyloxycarbonyl)phenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide

N-<4-(Benzyloxy)-3-(hydroxymethyl)phenyl>-1,4-dioxaspiro<4.5>decane-6-carboxamide

Downstream raw materials:

2-(Benzyloxy)-3-hydroxy-6-<<(trifluoromethyl)sulfonyl>oxy>-7,8,9,10-tetrahydrophenanthridine

2-(Benzyloxy)-3-hydroxy-7,8,9,10-tetrahydrophenanthridone