Synthesis of 3,3′-dimethyl-4,4′-diaminodiphenylmethane catalyzed by zeolites replacing mineral acids
✍ Scribed by Lin, Xiao; Zhao, Yingxian; Zhang, Shengjian; Wang, Lingyun; Wang, Yi; Guo, Yanna
- Book ID
- 125434801
- Publisher
- Elsevier Science
- Year
- 2014
- Tongue
- English
- Weight
- 445 KB
- Volume
- 45
- Category
- Article
- ISSN
- 1566-7367
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Selective terminal oxidation of 3,3-dimethyl-4-pentenoates does occur under chloride-free Wacker conditions [Pd(OAc)2/02] in AcOH to give 5-acetoxy-3.3-dimethyl-4pentenoates ( 7) and their analogues (2. 8) in good yields. Successive cyclization of 7 and 8 at vapor phase pyrolysis on SiO2 affords '3,
Oxidation of 4,4-dimethyl-Fkete triterpenoid with m-CPBA in presence of p-TsOH furnishes 3,4-aeco triterpenoid acid whereas 4-mono-methyl-3-keto-triterpenoid affords only the e-lactone under the identical condition.
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## Abstract magnified image Reaction of 3,5‐dimethyl‐4‐isoxazolyl‐diazonium tetrafluoroborate (**2**) with two equivalents of potassium acetate and five mole percent of 18‐crown‐6 in ethanol‐free chloroform produce 3‐methyl‐4__H__‐pyrazolo[3,4‐__d__]isoxazole (**3**) in good to excellent yield. Py