C₆₄H₇₉NO₁₄

Base Information

Chemical Name:C₆₄H₇₉NO₁₄
CAS No.:1526928-70-0
Molecular Formula:C₆₄H₇₉NO₁₄
Molecular Weight:1086.33
Hs Code.:

C<sub>64</sub>H<sub>79</sub>NO<sub>14</sub>

Synonyms:C₆₄H₇₉NO₁₄

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Chemical Property of C₆₄H₇₉NO₁₄

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Technology Process of C₆₄H₇₉NO₁₄

There total 7 articles about C₆₄H₇₉NO₁₄ 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: 73.0%

: 1443209-57-1
pillar[5]arene monocarboxylic acid

: 1526928-69-7
C₁₈H₃₁NO₃

: 1526928-70-0
C₆₄H₇₉NO₁₄

Guidance literature:: With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In dichloromethane; at -20 ℃; for 24h;
DOI:10.1039/c3cc48014c

Reference yield:

: 18598-23-7
ethyl (4-methoxyphenoxy)acetate

: 1526928-70-0
C₆₄H₇₉NO₁₄

Guidance literature:: Multi-step reaction with 3 steps

1.1: dichloromethane / 0.5 h / 20 °C

1.2: 3 h / 20 °C

2.1: sodium hydroxide / water; tetrahydrofuran / 4 h / 65 °C

3.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 24 h / -20 °C

With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; sodium hydroxide; In tetrahydrofuran; dichloromethane; water;
DOI:10.1039/c3cc48014c

Reference yield:

: C₁₈H₂₉N₃O₃

: 1526928-70-0
C₆₄H₇₉NO₁₄

Guidance literature:: Multi-step reaction with 2 steps

1: palladium on activated charcoal; hydrogen / methanol; chloroform / 24 h / Reflux

2: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; dmap / dichloromethane / 24 h / -20 °C

With dmap; palladium on activated charcoal; hydrogen; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; In methanol; dichloromethane; chloroform;
DOI:10.1039/c3cc48014c