C₃₅H₆₁NO₅

Base Information

Chemical Name:C₃₅H₆₁NO₅
CAS No.:1454597-79-5
Molecular Formula:C₃₅H₆₁NO₅
Molecular Weight:575.873
Hs Code.:

C<sub>35</sub>H<sub>61</sub>NO<sub>5</sub>

Synonyms:C₃₅H₆₁NO₅

Suppliers and Price of C₃₅H₆₁NO₅

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₃₅H₆₁NO₅

Chemical Property:

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Technology Process of C₃₅H₆₁NO₅

There total 21 articles about C₃₅H₆₁NO₅ 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: 98.0%

: 1454597-78-4
C₃₅H₅₉NO₅

: 1454597-79-5
C₃₅H₆₁NO₅

Guidance literature:: With [Ir(cod)(SIMes)(Pyr)]⁺PF₆^-; hydrogen; In dichloromethane; at 20 ℃; for 18h; under 67506.8 Torr; diastereoselective reaction; Autoclave;
DOI:10.1002/anie.201303776

Reference yield:

: (S)-Octadec-1-yn-3-ol

: 1454597-79-5
C₃₅H₆₁NO₅

Guidance literature:: Multi-step reaction with 7 steps

1.1: triphenylphosphine; di-isopropyl azodicarboxylate / tetrahydrofuran / 2 h / 0 °C / Inert atmosphere

2.1: water; sodium hydroxide / methanol / 1 h / Reflux

3.1: methyllithium / tetrahydrofuran / 0.67 h / -20 - 20 °C / Inert atmosphere

3.2: 1 h / 40 °C / Inert atmosphere

3.3: 0.25 h / 0 °C / Inert atmosphere

4.1: tert.-butyl lithium / diethyl ether; pentane / 0.17 h / -78 °C / Inert atmosphere

4.2: 2 h / -78 - 20 °C / Inert atmosphere

4.3: 2 h / 20 °C / Darkness

5.1: pyridine / dichloromethane / 1 h / 0 °C / Inert atmosphere

6.1: tetra-N-butylammonium tribromide / methanol / 4 h / 20 °C / Inert atmosphere

7.1: hydrogen; [Ir(cod)(SIMes)(Pyr)]⁺PF₆^- / dichloromethane / 18 h / 20 °C / 67506.8 Torr / Autoclave

With pyridine; di-isopropyl azodicarboxylate; [Ir(cod)(SIMes)(Pyr)]⁺PF₆^-; water; methyllithium; hydrogen; tert.-butyl lithium; tetra-N-butylammonium tribromide; triphenylphosphine; sodium hydroxide; In tetrahydrofuran; methanol; diethyl ether; dichloromethane; pentane;
DOI:10.1002/anie.201303776

Reference yield:

: 1354656-80-6
C₁₆H₃₆O₂Si

: 1454597-79-5
C₃₅H₆₁NO₅

Guidance literature:: Multi-step reaction with 5 steps

1.1: triphenylphosphine; iodine; 1H-imidazole / acetonitrile; diethyl ether / 0.5 h / 0 °C / Inert atmosphere

2.1: tert.-butyl lithium / diethyl ether; pentane / 0.17 h / -78 °C / Inert atmosphere

2.2: 2 h / -78 - 20 °C / Inert atmosphere

2.3: 2 h / 20 °C / Darkness

3.1: pyridine / dichloromethane / 1 h / 0 °C / Inert atmosphere

4.1: tetra-N-butylammonium tribromide / methanol / 4 h / 20 °C / Inert atmosphere

5.1: hydrogen; [Ir(cod)(SIMes)(Pyr)]⁺PF₆^- / dichloromethane / 18 h / 20 °C / 67506.8 Torr / Autoclave

With pyridine; 1H-imidazole; [Ir(cod)(SIMes)(Pyr)]⁺PF₆^-; hydrogen; iodine; tert.-butyl lithium; tetra-N-butylammonium tribromide; triphenylphosphine; In methanol; diethyl ether; dichloromethane; acetonitrile; pentane;
DOI:10.1002/anie.201303776