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WJPR Citation
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| All | Since 2020 | |
| Citation | 8502 | 4519 |
| h-index | 30 | 23 |
| i10-index | 227 | 96 |
A MODIFIED APPROACH FOR THE SYNTHESIS OF 2- CYCLOHEXYL-3-HYDROXY-1,4-NAPHTHOQUINONE (PARVAQUONE), ACCOMPLISHED WITH SYSTEMATIC PROCESS DEVELOPMENT STUDIES FOR SCALABILITY
Sanjay S. S.* and Shridhara K.
. Abstract In this work, a commercially affordable key starting material 2,3- dichloro-1,4-naphthoquinone 1 has been used for the synthesis of Parvaquone 2b with relatively better yield and purity. This raw material is readily available and can efficiently displace the costly raw material 2-chloro-1,4-naphthoquinone 6, which was predominantly used in the previous synthesis. This is novel and hither to unknown synthesis. The primary starting material cyclohexyl carboxylic acid 2 was reacted with 1 to generate 2a, which on hydrolysis resulted in the formation of 2b. The reaction conditions have been optimized, thus the present modified process can be easily scaled up and commercialized. Keywords: Parvaquone, Synthesis, Decarboxylation, Cyclohexylation, Hydrolysis, and Recovery. [Full Text Article] [Download Certificate] |
