C₂₄H₃₇NO₃

Base Information

Chemical Name:C₂₄H₃₇NO₃
CAS No.:1408154-77-7
Molecular Formula:C₂₄H₃₇NO₃
Molecular Weight:387.563
Hs Code.:

C<sub>24</sub>H<sub>37</sub>NO<sub>3</sub>

Synonyms:C₂₄H₃₇NO₃

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Chemical Property of C₂₄H₃₇NO₃

Chemical Property:

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Technology Process of C₂₄H₃₇NO₃

There total 9 articles about C₂₄H₃₇NO₃ 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: 95.0%

: 1408154-76-6
C₁₄H₂₈O₂

: 40217-17-2,90719-32-7,120574-96-1,102029-44-7
(R)-4-(phenylmethyl)-2-oxazolidinone

: 1408154-77-7
C₂₄H₃₇NO₃

Guidance literature:: With pivaloyl chloride; triethylamine; lithium chloride; In tetrahydrofuran; at -20 - 0 ℃;
DOI:10.1016/j.tetlet.2012.08.112

Reference yield:

: C₂₃H₄₂O₄SSi

: 1408154-77-7
C₂₄H₃₇NO₃

Guidance literature:: Multi-step reaction with 8 steps

1: dilithium tetrachlorocuprate / diethyl ether / -78 °C

2: tetrabutyl ammonium fluoride / tetrahydrofuran / 0 °C

3: oxalyl dichloride; dimethyl sulfoxide; triethylamine / dichloromethane / -78 °C

5: diisobutylaluminium hydride / dichloromethane / -78 °C

6: 10 wt% Pd(OH)2 on carbon; triethylamine / benzene / 20 °C

7: sodium chlorite; sodium dihydrogenphosphate / water; tert-butyl alcohol / 20 °C

8: pivaloyl chloride; triethylamine; lithium chloride / tetrahydrofuran / -20 - 0 °C

With sodium chlorite; sodium dihydrogenphosphate; oxalyl dichloride; dilithium tetrachlorocuprate; 10 wt% Pd(OH)2 on carbon; tetrabutyl ammonium fluoride; pivaloyl chloride; diisobutylaluminium hydride; dimethyl sulfoxide; triethylamine; lithium chloride; In tetrahydrofuran; diethyl ether; dichloromethane; water; tert-butyl alcohol; benzene; 1: |Grignard Reaction / 3: |Swern Oxidation / 4: |Wittig Olefination;
DOI:10.1016/j.tetlet.2012.08.112

Reference yield:

: C₁₄H₂₈O

: 1408154-77-7
C₂₄H₃₇NO₃

Guidance literature:: Multi-step reaction with 3 steps

1: 10 wt% Pd(OH)2 on carbon; triethylamine / benzene / 20 °C

2: sodium chlorite; sodium dihydrogenphosphate / water; tert-butyl alcohol / 20 °C

3: pivaloyl chloride; triethylamine; lithium chloride / tetrahydrofuran / -20 - 0 °C

With sodium chlorite; sodium dihydrogenphosphate; 10 wt% Pd(OH)2 on carbon; pivaloyl chloride; triethylamine; lithium chloride; In tetrahydrofuran; water; tert-butyl alcohol; benzene;
DOI:10.1016/j.tetlet.2012.08.112