C₂₄H₃₆O₅

Base Information

Chemical Name:C₂₄H₃₆O₅
CAS No.:122131-35-5
Molecular Formula:C₂₄H₃₆O₅
Molecular Weight:404.547
Hs Code.:

C<sub>24</sub>H<sub>36</sub>O<sub>5</sub>

Synonyms:C₂₄H₃₆O₅

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Chemical Property of C₂₄H₃₆O₅

Chemical Property:

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Technology Process of C₂₄H₃₆O₅

There total 20 articles about C₂₄H₃₆O₅ 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: 97.0%

: 122131-34-4
C₂₆H₃₈O₆

: 122131-35-5
C₂₄H₃₆O₅

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether;
DOI:10.1016/S0040-4039(00)82126-7

Reference yield:

: 100-39-0
benzyl bromide

: 122131-35-5
C₂₄H₃₆O₅

Guidance literature:: Multi-step reaction with 16 steps

2: 92 percent / LDA / tetrahydrofuran / 0.04 h / -78 °C

3: 75 percent / 1) LDA, 2) CF₃COOH / tetrahydrofuran / -78 °C

4: 83 percent / LiAlH₄ / tetrahydrofuran / -30 °C

5: 95 percent / pyridine

6: 92 percent / NaH / tetrahydrofuran

7: 1) Zn-Cu, 2) Zn, NH₄Cl / 1) ether, room temperature, 5.5 h; 2) MeOH, 0 deg C

8: 74 percent / methanol / Ambient temperature

9: NaBH₄ / methanol

10: 1) MsCl, pyridine; 2) t-BuOK / 2) DMSO

11: 89 percent / HgCl₂ / acetonitrile; H₂O / 40 °C

12: TsOH

13: PCC, MS-3A

14: CH₂Cl₂

15: NaBH₄, NiCl₂*6H₂O / methanol

16: 97 percent / LiAlH₄ / diethyl ether

With pyridine; sodium tetrahydroborate; lithium aluminium tetrahydride; potassium tert-butylate; copper; sodium hydride; ammonium chloride; toluene-4-sulfonic acid; methanesulfonyl chloride; pyridinium chlorochromate; trifluoroacetic acid; mercury dichloride; nickel dichloride; zinc; lithium diisopropyl amide; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; acetonitrile;
DOI:10.1016/S0040-4039(00)82126-7

Reference yield:

: 116217-06-2
(3aR,4R,7aS)-2-Oxo-2,3,3a,4,5,7a-hexahydro-benzofuran-4-carboxylic acid

: 122131-35-5
C₂₄H₃₆O₅

Guidance literature:: Multi-step reaction with 16 steps

2: 92 percent / LDA / tetrahydrofuran / 0.04 h / -78 °C

3: 75 percent / 1) LDA, 2) CF₃COOH / tetrahydrofuran / -78 °C

4: 83 percent / LiAlH₄ / tetrahydrofuran / -30 °C

5: 95 percent / pyridine

6: 92 percent / NaH / tetrahydrofuran

7: 1) Zn-Cu, 2) Zn, NH₄Cl / 1) ether, room temperature, 5.5 h; 2) MeOH, 0 deg C

8: 74 percent / methanol / Ambient temperature

9: NaBH₄ / methanol

10: 1) MsCl, pyridine; 2) t-BuOK / 2) DMSO

11: 89 percent / HgCl₂ / acetonitrile; H₂O / 40 °C

12: TsOH

13: PCC, MS-3A

14: CH₂Cl₂

15: NaBH₄, NiCl₂*6H₂O / methanol

16: 97 percent / LiAlH₄ / diethyl ether

With pyridine; sodium tetrahydroborate; lithium aluminium tetrahydride; potassium tert-butylate; copper; sodium hydride; ammonium chloride; toluene-4-sulfonic acid; methanesulfonyl chloride; pyridinium chlorochromate; trifluoroacetic acid; mercury dichloride; nickel dichloride; zinc; lithium diisopropyl amide; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; water; acetonitrile;
DOI:10.1016/S0040-4039(00)82126-7