反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
The product of Step 3a (750 mg, 4 mmol) is dissolved in a mixture of THF, t-BuOH, and water (2:1:1, 60 mL). KH2PO4 (1.36 g, 10 mmol) is added followed by NaClO2 (900 mg, 10 mmol). The mixture is stirred at rt for 5 days. Aqueous NaOH (2M, 10 mL) is added, and a majority of the organic solvents are removed in vacuo yielding an aqueous suspension. This suspension is diluted with water and washed three times with CH2Cl2. The aqueous layer is acidified to pH<6 with 25% H2SO4 and the product is extracted three times with CH2Cl2. The combined organic washes are dried over Na2SO4, filtered and concentrated in vacuo to yield 5-phenylthiophene-2-carboxylic acid (417 mg, 51%). MS for C11H8O2S (ESI) (M−H)− m/z 203.
WORKUP
后处理
- customa majority of the organic solvents are removed in vacuo
- customyielding an aqueous suspension
- washwashed three times with CH2Cl2
- extractionthe product is extracted three times with CH2Cl2
- dry with materialThe combined organic washes are dried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo