Extended knowledge of 35963-20-3

Do you like my blog? If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 35963-20-3, COA of Formula: https://www.ambeed.com/products/35963-20-3.html.

New Advances in Chemical Research in 2021. Chemistry is a science major with cience and engineering. The main research directions are chemical synthesis, and research on the structure and performance of functional materials. 35963-20-3, Name is ((1R,4S)-7,7-Dimethyl-2-oxobicyclo[2.2.1]heptan-1-yl)methanesulfonic acid, SMILES is O=S(C[C@]1(C2(C)C)C(C[C@]2([H])CC1)=O)(O)=O, in an article , author is SATO, H, once mentioned of 35963-20-3, HPLC of Formula: https://www.ambeed.com/products/35963-20-3.html.

A practical procedure for synthesis of a new uricosuric agent, 5-chloro-7,8-dihydro-3-phenylfuro[2,3-g]-1,2-benzisoxazole-7-carboxylic acid (1, AA-193) is described, which starts from 2,5-dichlorophenol (3b) and involves 5-chloro-6-hydroxy-3-phenyl-1,2-benzisoxazole (2) as the key intermediate. Successive treatment of 3b with benzoyl chloride-aluminum chloride (AlCl3) and hot ethanolic sodium hydroxide gives 4-benzoyl-2,5-dichlorophenol (8, 61%), which is oximated with hydroxylamine hydrochloride and then transformed into the benzisoxazole 2 (88%) with potassium hydroxide in N,N-dimethylformamide (DMF) (method C). The reaction of 2 with aqueous formaldehyde and dimethylamine affords the Mannich base Ila (97%), which is treated with a sulfonium ylide 12, 14 or 15 followed by heating with sodium hydroxide (NaOH) in ethanol (EtOH) to give 1 in high yield (method E).

Do you like my blog? If you like, you can also browse other articles about this kind. Thanks for taking the time to read the blog about 35963-20-3, COA of Formula: https://www.ambeed.com/products/35963-20-3.html.

Reference:
Benzisoxazole – Wikipedia,
,Benzisoxazole – an overview | ScienceDirect Topics