HRID328430

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID94109

Benzamide, N,N-bis(2-hydroxyethyl)-

C11H15NO3

$结构：CCCCCCCC/C=C\CCCCCCCCCCCC(=O)Cl$

HCID5364502

未命名化合物

PRODUCTS

生成物

$结构：CCCCCCCC/C=C\CCCCCCCCCCCC(=O)OCCN(CCOC(=O)CCCCCCCCCCC/C=C\CCCCCCCC)C(=O)c1ccccc1$

HCID54598631

(Benzoylazanediyl)di(ethane-2,1-diyl) (13Z,13'Z)di-docos-13-enoate

C55H95NO5

PROCEDURE

实验过程

N,N-bis(2-erucoyloxyethyl)benzamid was prepared by the procedure of example 1 from 19.5 gms. (0.1 mole) of N,N-bis(2-hydroxyethyl)benzamide and 71 gms. (0.2 mole) of erucoyl chloride. The structure of the final product was characterized on the basis of IR and NMR spectral analyses as described in example 1.

WORKUP

后处理

customN,N-bis(2-erucoyloxyethyl)benzamid was prepared by the procedure of example 1 from 19.5 gms

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-7c54b5e1adc2457296b177b2a1af74e6
来源数据集: uspto-grants-1977_04
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04017522
来源说明: uspto-grants-1977_04

反应 SMILES

[OH:1][CH2:2][CH2:3][N:4]([CH2:13][CH2:14][OH:15])[C:5](=[O:12])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[C:16](Cl)(=[O:38])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27]/[CH:28]=[CH:29]\[CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH3:37]>>[C:16]([O:1][CH2:2][CH2:3][N:4]([CH2:13][CH2:14][O:15][C:16](=[O:38])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27]/[CH:28]=[CH:29]\[CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH3:37])[C:5](=[O:12])[C:6]1[CH:7]=[CH:8][CH:9]=[CH:10][CH:11]=1)(=[O:38])[CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27]/[CH:28]=[CH:29]\[CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH3:37]