N¹,N⁸-bis(2-acetoxybenzoyl)-N¹,N⁸-bis(2-benzyloxy)-3,6-dioxa-1,8-octanediamine

Base Information

Chemical Name:N¹,N⁸-bis(2-acetoxybenzoyl)-N¹,N⁸-bis(2-benzyloxy)-3,6-dioxa-1,8-octanediamine
CAS No.:241147-47-7
Molecular Formula:C₃₈H₄₀N₂O₁₀
Molecular Weight:684.743
Hs Code.:

N<sup>1</sup>,N<sup>8</sup>-bis(2-acetoxybenzoyl)-N<sup>1</sup>,N<sup>8</sup>-bis(2-benzyloxy)-3,6-dioxa-1,8-octanediamine

Synonyms:N¹,N⁸-bis(2-acetoxybenzoyl)-N¹,N⁸-bis(2-benzyloxy)-3,6-dioxa-1,8-octanediamine

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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 N¹,N⁸-bis(2-acetoxybenzoyl)-N¹,N⁸-bis(2-benzyloxy)-3,6-dioxa-1,8-octanediamine

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Technology Process of N¹,N⁸-bis(2-acetoxybenzoyl)-N¹,N⁸-bis(2-benzyloxy)-3,6-dioxa-1,8-octanediamine

There total 4 articles about N¹,N⁸-bis(2-acetoxybenzoyl)-N¹,N⁸-bis(2-benzyloxy)-3,6-dioxa-1,8-octanediamine 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: 89.0%

: 98902-91-1
N¹,N⁸-bis(benzyloxy)-3,6-dioxa-1,8-octanediamine

: 5538-51-2
O-acetylsalicyloyl chloride

: 241147-47-7
N¹,N⁸-bis(2-acetoxybenzoyl)-N¹,N⁸-bis(2-benzyloxy)-3,6-dioxa-1,8-octanediamine

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; for 4h; Ambient temperature;
DOI:10.1021/jm980611q

Reference yield:

: 79722-21-7
tert-butyl N-(benzyloxy)carbamate

: 241147-47-7
N¹,N⁸-bis(2-acetoxybenzoyl)-N¹,N⁸-bis(2-benzyloxy)-3,6-dioxa-1,8-octanediamine

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) NaH / 1.) DMF, RT, 40 min, 2.) DMF, 53 deg C, 21 h

2: 84 percent / conc. HCl / methanol / 20 h / Ambient temperature

3: 89 percent / DIEA / CH₂Cl₂ / 4 h / Ambient temperature

With hydrogenchloride; sodium hydride; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane;
DOI:10.1021/jm980611q

Reference yield:

: 112-26-5,27252-69-3
1,2-bis(2-chloroethoxy)ethane

: 241147-47-7
N¹,N⁸-bis(2-acetoxybenzoyl)-N¹,N⁸-bis(2-benzyloxy)-3,6-dioxa-1,8-octanediamine

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) NaH / 1.) DMF, RT, 40 min, 2.) DMF, 53 deg C, 21 h

2: 84 percent / conc. HCl / methanol / 20 h / Ambient temperature

3: 89 percent / DIEA / CH₂Cl₂ / 4 h / Ambient temperature

With hydrogenchloride; sodium hydride; N-ethyl-N,N-diisopropylamine; In methanol; dichloromethane;
DOI:10.1021/jm980611q