HRID279923

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2771642

3-(Trimethylsilyl)ethynylbenzaldehyde

C12H14OSi

结构：Nc1cc(C(c2ccc(Nc3ccccc3)c(N)c2)(C(F)(F)F)C(F)(F)F)ccc1Nc1ccccc1

HCID14205049

未命名化合物

HCID23665763

Sodium Bisulfite

HNaO3S

PRODUCTS

生成物

结构：C#Cc1cccc(-c2nc3cc(C(c4ccc5c(c4)nc(-c4cccc(C#C)c4)n5-c4ccccc4)(C(F)(F)F)C(F)(F)F)ccc3n2-c2ccccc2)c1

HCID23322967

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID19096565

未命名化合物

PROCEDURE

实验过程

The exact procedure described above (high dilution and dropwise addition) was repeated for 26.0 g of the aldehyde (VI), 110 g of sodium bisulfite, and 30.0 g of the tetramine (V) in a total volume of 4.5 L of 1:5 water-ethanol. At the end, the powdery end product (VIII) was fractionated by Soxhlet extraction into an ether-insoluble portion (high oligomers) and an ether-soluble portion (20.0 g, 46.9%). The latter material, when tested on the Kofler hot bench at 250° C., showed a gel time of about 3 minutes.

WORKUP

后处理

additionhigh dilution and dropwise addition)
extractionAt the end, the powdery end product (VIII) was fractionated by Soxhlet extraction into an ether-insoluble portion (high oligomers)
customtested on the Kofler hot bench at 250° C.
customa gel time of about 3 minutes

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-f92c3db8dba24f3b96fe28d214e8bee8
来源数据集: uspto-grants-1986_05
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04587315
来源说明: uspto-grants-1986_05

反应 SMILES

C[Si]([C:5]#[C:6][C:7]1[CH:8]=[C:9]([CH:12]=[CH:13][CH:14]=1)[CH:10]=O)(C)C.S(=O)(O)[O-].[Na+].[NH2:20][C:21]1[CH:22]=[C:23]([C:34]([C:43]2[CH:48]=[CH:47][C:46]([NH:49][C:50]3[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=3)=[C:45]([NH2:56])[CH:44]=2)([C:39]([F:42])([F:41])[F:40])[C:35]([F:38])([F:37])[F:36])[CH:24]=[CH:25][C:26]=1[NH:27][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1>O.C(O)C>[F:36][C:35]([F:37])([F:38])[C:34]([C:23]1[CH:24]=[CH:25][C:26]2[N:27]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)[C:10]([C:9]3[CH:12]=[CH:13][CH:14]=[C:7]([C:6]#[CH:5])[CH:8]=3)=[N:20][C:21]=2[CH:22]=1)([C:43]1[CH:48]=[CH:47][C:46]2[N:49]([C:50]3[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=3)[C:10]([C:9]3[CH:12]=[CH:13][CH:14]=[C:7]([C:6]#[CH:5])[CH:8]=3)=[N:56][C:45]=2[CH:44]=1)[C:39]([F:40])([F:41])[F:42]