HRID1734772

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CC(C)(C)c1cc(C(C)(C)C)c(O)c(C(C)(C)C)c1

HCID12902

2,4,6-Tris(tert-butyl)phenol

C18H30O

HCID12532795

1,3-Di-tert-butyl-2,4-dichloro-1,3,2,4-diazadiphosphetidine

C8H18Cl2N2P2

PRODUCTS

生成物

结构：CC(C)(C)c1cc(C(C)(C)C)c(OP2N(C(C)(C)C)P(Oc3c(C(C)(C)C)cc(C(C)(C)C)cc3C(C)(C)C)N2C(C)(C)C)c(C(C)(C)C)c1

HCID19438413

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID8471

Triethylamine

C6H15N

PROCEDURE

实验过程

The procedure of Example 1 is repeated using 2,4-dichloro-1,3-di-tert-butyl-1,3,2,4-diazadiphosphetidine, 2,4,6-tri-tert-butylphenol and triethylamine to give the title compound.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-55dc06b118ee4b3291821c3c9277e819
来源数据集: uspto-grants-1996_07
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05534646
来源说明: uspto-grants-1996_07

反应 SMILES

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