HRID2346241

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID5395

1,4-Dihydroxy-2,2,6,6-tetramethylpiperidine

C9H19NO2

HCID8471

Triethylamine

C6H15N

HCID24387

Phosphorous trichloride

Cl3P

结构：CC(c1cc(C(C)(C)C)cc(C(C)(C)C)c1O)c1cc(C(C)(C)C)cc(C(C)(C)C)c1O

HCID118899

Tetrabutyl ethylidenebisphenol

C30H46O2

PRODUCTS

生成物

结构：CC1c2cc(C(C)(C)C)cc(C(C)(C)C)c2OP(OC2CC(C)(C)N(O)C(C)(C)C2)Oc2c1cc(C(C)(C)C)cc2C(C)(C)C

HCID21273724

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-e3a6a241c2f343119f5b2965d6dbe75c
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (10/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (10/10)

反应 SMILES

[CH3:49][CH2:50][N:51]([CH2:52][CH3:53])[CH2:54][CH3:55].[CH:5]([CH3:6])([c:7]1[c:8]([OH:21])[c:9]([C:17]([CH3:18])([CH3:19])[CH3:20])[cH:10][c:11]([C:13]([CH3:14])([CH3:15])[CH3:16])[cH:12]1)[c:22]1[c:23]([OH:36])[c:24]([C:32]([CH3:33])([CH3:34])[CH3:35])[cH:25][c:26]([C:28]([CH3:29])([CH3:30])[CH3:31])[cH:27]1.[OH:37][N:38]1[C:39]([CH3:47])([CH3:48])[CH2:40][CH:41]([OH:46])[CH2:42][C:43]1([CH3:44])[CH3:45].[P:1]([Cl:2])([Cl:3])[Cl:4]>>[P:1]1([O:46][CH:41]2[CH2:40][C:39]([CH3:47])([CH3:48])[N:38]([OH:37])[C:43]([CH3:44])([CH3:45])[CH2:42]2)[O:21][c:8]2[c:7]([cH:12][c:11]([C:13]([CH3:14])([CH3:15])[CH3:16])[cH:10][c:9]2[C:17]([CH3:18])([CH3:19])[CH3:20])[CH:5]([CH3:6])[c:22]2[c:23]([c:24]([C:32]([CH3:33])([CH3:34])[CH3:35])[cH:25][c:26]([C:28]([CH3:29])([CH3:30])[CH3:31])[cH:27]2)[O:36]1