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HRID2403047

反应详情

EQUATION

反应方程式

HRID 2403047 的结构方程式

REACTANTS

反应物

3
反应SMILES：O=C([O-])[O-].[Na+].[Na+]
HCID10340

Carbonic acid sodium salt (1:2)

CNa2O3

反应SMILES：Cc1sc(B(O)O)cc1Br
HCID12184011

(4-Bromo-5-methylthiophen-2-yl)boronic acid

C5H6BBrO2S

反应SMILES：Oc1ccc(Br)s1
HCID21108627

5-Bromothiophene-2-ol

C4H3BrOS

PRODUCTS

产物

1
反应SMILES：Cc1sc(-c2cc(O)cs2)cc1Br
HCID67309403

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

2
反应SMILES：c1ccc([P](c2ccccc2)(c2ccccc2)[Pd]([P](c2ccccc2)(c2ccccc2)c2ccccc2)([P](c2ccccc2)(c2ccccc2)c2ccccc2)[P](c2ccccc2)(c2ccccc2)c2ccccc2)cc1
催化剂HCID178418397

未命名化合物

反应SMILES：C1CCOC1
溶剂HCID8028

Tetrahydrofuran

C4H8O

PROCEDURE

实验过程

Compound 3 is mixed with 5-bromothiophen-2-ol in the presence of tetrakis(triphenylphosphine)palladium(0) [Pd(PPh3)4] and Na2CO3 in tetrahydrofuran (THF) for 24 h at 80° C. The crude product is distillated in vacuo and purified by silica-gel column chromatography (eluent:hexane). Compound 5 (5.01 g) is obtained as a yellowish solid.

WORKUP

后处理

  1. custompurified by silica-gel column chromatography (eluent:hexane)