HRID918108

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID75550

1,4-Benzenediol, 2,6-bis(1,1-dimethylethyl)-

C14H22O2

HCID4104741

Docosanoyl chloride

C22H43ClO

PRODUCTS

生成物

结构：CCCCCCCCCCCCCCCCCCCCCC(=O)Oc1cc(C(C)(C)C)c(O)c(C(C)(C)C)c1

HCID53937426

未命名化合物

PROCEDURE

实验过程

The procedure of Example 1 is repeated except that 2,6-di-t-butylhydroquinone and docosanoyl chloride were employed to yield the above named product. It has a melting point of 59°-61°C.

WORKUP

后处理

customto yield the above named product

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-f55c29ae628241078c93c473cefd3054
来源数据集: uspto-grants-1976_07
DOI: 10.6084/m9.figshare.5104873.v1
专利: US03969383
来源说明: uspto-grants-1976_07

反应 SMILES

[C:1]([C:5]1[CH:11]=[C:10]([OH:12])[CH:9]=[C:8]([C:13]([CH3:16])([CH3:15])[CH3:14])[C:6]=1[OH:7])([CH3:4])([CH3:3])[CH3:2].[C:17](Cl)(=[O:39])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH3:38]>>[C:17]([O:12][C:10]1[CH:11]=[C:5]([C:1]([CH3:4])([CH3:3])[CH3:2])[C:6]([OH:7])=[C:8]([C:13]([CH3:16])([CH3:15])[CH3:14])[CH:9]=1)(=[O:39])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH2:37][CH3:38]