C₃₀H₄₉NO₅

Base Information

Chemical Name:C₃₀H₄₉NO₅
CAS No.:1403235-37-9
Molecular Formula:C₃₀H₄₉NO₅
Molecular Weight:503.723
Hs Code.:

C<sub>30</sub>H<sub>49</sub>NO<sub>5</sub>

Synonyms:C₃₀H₄₉NO₅

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Chemical Property of C₃₀H₄₉NO₅

Chemical Property:

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Technology Process of C₃₀H₄₉NO₅

There total 10 articles about C₃₀H₄₉NO₅ 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:

: 1403235-24-4
C₂₀H₃₄O₂

: 1123186-20-8
C₁₇H₁₈Cl₃NO₅

: 1403235-37-9
C₃₀H₄₉NO₅

Guidance literature:: With dmap; In toluene; at 20 ℃; for 3h; Inert atmosphere;
DOI:10.1021/ol302309c

Reference yield:

: 1403235-36-8
C₁₄H₂₀O

: 1403235-37-9
C₃₀H₄₉NO₅

Guidance literature:: Multi-step reaction with 8 steps

1.1: 4-methylmorpholine N-oxide; osmium(VIII) oxide / tert-butyl alcohol; water; tetrahydrofuran / 12 h / Inert atmosphere

1.2: 3 h / 0 - 20 °C / Inert atmosphere

2.1: di-n-butylboryl trifluoromethanesulfonate / dichloromethane / 0.17 h / 0 °C / Inert atmosphere

2.2: 1 h / 0 °C / Inert atmosphere

2.3: 6 h / -78 - 0 °C / Inert atmosphere

3.1: 2,6-dimethylpyridine / dichloromethane / 0.5 h / 0 °C / Inert atmosphere

4.1: sodium tetrahydroborate / water; tetrahydrofuran / 0 - 20 °C / Inert atmosphere

5.1: triethylamine; dmap / dichloromethane / 0 - 20 °C / Inert atmosphere

6.1: copper dichloride; 1-Phenylprop-1-yne / tetrahydrofuran / 24 h / Inert atmosphere; Reflux

7.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 °C / Inert atmosphere

8.1: dmap / toluene / 3 h / 20 °C / Inert atmosphere

With 2,6-dimethylpyridine; 1-Phenylprop-1-yne; dmap; sodium tetrahydroborate; osmium(VIII) oxide; di-n-butylboryl trifluoromethanesulfonate; tetrabutyl ammonium fluoride; 4-methylmorpholine N-oxide; triethylamine; copper dichloride; In tetrahydrofuran; dichloromethane; water; toluene; tert-butyl alcohol; 2.1: |Evans Aldol Reaction / 2.2: |Evans Aldol Reaction / 2.3: |Evans Aldol Reaction;
DOI:10.1021/ol302309c

Reference yield:

: 82538-49-6
(3S)-5-(benzyloxy)-3-methylpentanal

: 1403235-37-9
C₃₀H₄₉NO₅

Guidance literature:: Multi-step reaction with 7 steps

1.1: di-n-butylboryl trifluoromethanesulfonate / dichloromethane / 0.17 h / 0 °C / Inert atmosphere

1.2: 1 h / 0 °C / Inert atmosphere

1.3: 6 h / -78 - 0 °C / Inert atmosphere

2.1: 2,6-dimethylpyridine / dichloromethane / 0.5 h / 0 °C / Inert atmosphere

3.1: sodium tetrahydroborate / water; tetrahydrofuran / 0 - 20 °C / Inert atmosphere

4.1: triethylamine; dmap / dichloromethane / 0 - 20 °C / Inert atmosphere

5.1: copper dichloride; 1-Phenylprop-1-yne / tetrahydrofuran / 24 h / Inert atmosphere; Reflux

6.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 20 °C / Inert atmosphere

7.1: dmap / toluene / 3 h / 20 °C / Inert atmosphere

With 2,6-dimethylpyridine; 1-Phenylprop-1-yne; dmap; sodium tetrahydroborate; di-n-butylboryl trifluoromethanesulfonate; tetrabutyl ammonium fluoride; triethylamine; copper dichloride; In tetrahydrofuran; dichloromethane; water; toluene; 1.1: |Evans Aldol Reaction / 1.2: |Evans Aldol Reaction / 1.3: |Evans Aldol Reaction;
DOI:10.1021/ol302309c