HRID64937

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID70370

2,6-Di-tert-butyl-4-mercaptophenol

C14H22OS

HCID73219

3,5-Di-tert-butyl-4-hydroxybenzaldehyde

C15H22O2

PRODUCTS

生成物

结构：CC(C)(C)c1cc(SC(Sc2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)c2cc(C(C)(C)C)c(O)c(C(C)(C)C)c2)cc(C(C)(C)C)c1O

HCID13710008

未命名化合物

收率 87%

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID887

Methanol

CH4O

2 次

PROCEDURE

实验过程

The procedure of Example 1 is repeated using 23.84 grams of 2,6-di-tert-butyl-4-mercaptophenol, 11.72 grams of 3,5-di-tert-butyl-4-hydroxybenzaldehyde and 150 ml of methyl alcohol. Trituration with methyl alcohol gives 30 grams (87% yield) of white crystals, mp 175°-177° C.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-36a37f1261b44d6ab252646882ffa253
来源数据集: uspto-grants-1986_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04611023
来源说明: uspto-grants-1986_09

反应 SMILES

[C:1]([C:5]1[CH:10]=[C:9]([SH:11])[CH:8]=[C:7]([C:12]([CH3:15])([CH3:14])[CH3:13])[C:6]=1[OH:16])([CH3:4])([CH3:3])[CH3:2].[C:17]([C:21]1[CH:22]=[C:23]([CH:26]=[C:27]([C:30]([CH3:33])([CH3:32])[CH3:31])[C:28]=1[OH:29])[CH:24]=O)([CH3:20])([CH3:19])[CH3:18]>CO>[C:1]([C:5]1[CH:10]=[C:9]([S:11][CH:24]([S:11][C:9]2[CH:8]=[C:7]([C:12]([CH3:13])([CH3:14])[CH3:15])[C:6]([OH:16])=[C:5]([C:1]([CH3:4])([CH3:3])[CH3:2])[CH:10]=2)[C:23]2[CH:22]=[C:21]([C:17]([CH3:18])([CH3:20])[CH3:19])[C:28]([OH:29])=[C:27]([C:30]([CH3:31])([CH3:32])[CH3:33])[CH:26]=2)[CH:8]=[C:7]([C:12]([CH3:15])([CH3:14])[CH3:13])[C:6]=1[OH:16])([CH3:4])([CH3:3])[CH3:2]