C₅₀H₆₂O₁₈

Base Information

Chemical Name:C₅₀H₆₂O₁₈
CAS No.:1339943-42-8
Molecular Formula:C₅₀H₆₂O₁₈
Molecular Weight:951.031
Hs Code.:

C<sub>50</sub>H<sub>62</sub>O<sub>18</sub>

Synonyms:C₅₀H₆₂O₁₈

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Chemical Property of C₅₀H₆₂O₁₈

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Technology Process of C₅₀H₆₂O₁₈

There total 20 articles about C₅₀H₆₂O₁₈ 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:

: 1339943-40-6
C₅₆H₇₆O₁₈Si

: 1339943-42-8
C₅₀H₆₂O₁₈

Guidance literature:: With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 20 ℃; for 24h;

Reference yield:

: 31139-02-3,31139-03-4,56124-48-2,88335-93-7,88335-94-8,93603-11-3
(1R,6S)-6-methoxycarbonyl-3-cyclohexene-1-carboxylic acid

: 1339943-42-8
C₅₀H₆₂O₁₈

Guidance literature:: Multi-step reaction with 10 steps

1.1: phosgene / N,N-dimethyl-formamide / dichloromethane / 3 h / 20 °C

1.2: 3.33 h / Reflux

2.1: sodium hydroxide / water / 20 °C / pH 7 / Aqueous phosphate buffer

3.1: potassium iodide; sodium hydrogencarbonate; iodine / water / 24 h / 0 - 20 °C

4.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 h / Reflux

5.1: sodium hydrogencarbonate / 12 h / 20 °C / Inert atmosphere

6.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 12 h

7.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 17 h / 10 - 20 °C

8.1: methyllithium; boron trifluoride diethyl etherate; copper(l) cyanide / diethyl ether; tetrahydrofuran / -78 °C

9.1: dichloromethane / 2 h / 20 °C / Molecular sieve; Inert atmosphere

9.2: 0.25 h

9.3: 2 h / Inert atmosphere

10.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 24 h / 20 °C

With phosgene; boron trifluoride diethyl etherate; tetrabutyl ammonium fluoride; methyllithium; iodine; copper(l) cyanide; sodium hydrogencarbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; 3-chloro-benzenecarboperoxoic acid; potassium iodide; sodium hydroxide; N,N-dimethyl-formamide; In tetrahydrofuran; diethyl ether; dichloromethane; water;

Reference yield:

: 4841-84-3
dimethyl cis-1,2,3,6-tetrahydrophthalate

: 1339943-42-8
C₅₀H₆₂O₁₈

Guidance literature:: Multi-step reaction with 11 steps

1.1: sodium hydroxide / water / 20 °C / pH 7 / Aqueous phosphate buffer

2.1: phosgene / N,N-dimethyl-formamide / dichloromethane / 3 h / 20 °C

2.2: 3.33 h / Reflux

3.1: sodium hydroxide / water / 20 °C / pH 7 / Aqueous phosphate buffer

4.1: potassium iodide; sodium hydrogencarbonate; iodine / water / 24 h / 0 - 20 °C

5.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / tetrahydrofuran / 20 h / Reflux

6.1: sodium hydrogencarbonate / 12 h / 20 °C / Inert atmosphere

7.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 12 h

8.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 17 h / 10 - 20 °C

9.1: methyllithium; boron trifluoride diethyl etherate; copper(l) cyanide / diethyl ether; tetrahydrofuran / -78 °C

10.1: dichloromethane / 2 h / 20 °C / Molecular sieve; Inert atmosphere

10.2: 0.25 h

10.3: 2 h / Inert atmosphere

11.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 24 h / 20 °C

With phosgene; boron trifluoride diethyl etherate; tetrabutyl ammonium fluoride; methyllithium; iodine; copper(l) cyanide; sodium hydrogencarbonate; 1,8-diazabicyclo[5.4.0]undec-7-ene; 3-chloro-benzenecarboperoxoic acid; potassium iodide; sodium hydroxide; N,N-dimethyl-formamide; In tetrahydrofuran; diethyl ether; dichloromethane; water;