592-33-6

Upstream product

• 127-08-2 potassium acetate 
• 64-19-7 acetic acid 
• 109-70-6 1.3-chlorobromopropane 
• 626-68-6 2-methyl-[1,3]dioxane 
• 6543-17-5 2,2-diethyl-1,3-dioxane 
• 506-96-7 Acetyl bromide 
• 23277-12-5 tetrahydro-2-methyl-2-furyl hydroperoxide 

Downstream Products

• 503-30-0 trimethylene oxide 
• 73974-93-3 3-(2-oxocyclohexyl)propyl acetate 
• 16120-95-9 4-tert.-Butyl-2-(3-acetoxy-propyl)-cyclohexanon 
• 4339-94-0 3-(dimethylamino)-1-propyl acetate 
• 616236-63-6 Acetic acid 3-imidazol-1-yl-propyl ester 
• 112859-68-4 Acetic acid 3-(3-formyl-4-nitro-phenoxy)-propyl ester 
• 1705-77-7 2,2-diphenyl-5-acetoxyvaleronitrile 
• 80015-01-6 diethyl N-<4-<(3-acetoxypropyl)amino>benzoyl>-L-glutamate 
• 129175-74-2 diethyl N-<4-<(3-acetoxypropyl)amino>-3-fluorobenzoyl>-L-glutamate 
• 87010-30-8 3-(2-oxo-1,3-oxazolidin-3-yl)-propylacetate 
• 321722-24-1 acetic acid 3-[5-(4-bromo-benzyl)-7-(3,5-dichloro-phenyl)-5-methyl-6-oxo-6,7-dihydro-5H-imidazo[1,2-a]imidazole-3-sulfonyl]-propyl ester 
• 437763-89-8 acetic acid 3-[3-(3-amino-1-butyl-2-oxo-1,2-dihydro-[1,8]naphthyridin-4-yl)-phenoxy]-propyl ester 
• 112859-59-3 (Z,E)-3-<3-<(2,4-dioxoimidazolidin-5-ylidene)methyl>-4-nitrophenoxy>propyl acetate 
• 125314-97-8 3-<1-(3-acetoxypropyl)-3-indolyl>-4-(1-methyl-3-indolyl)-2,5-furandione 

Relevant academic research and scientific papers

Effect of Crown Ethers on Bromination of 2-Methyl-1,3-dioxacycloalkanes with N-Bromosuccinimide

Crown ethers exert a pronounced catalytic effect on bromination of 2-methyl-1,3-dioxacycloalkanes with N-bromosuccinimide and increase the yield of 2-bromomethyl derivatives.

Reactions of 1,3-Dioxacyclanes with Acid Halides. A New Synthesis for ω-Halohydrine Esters

Reaction of 1,3-dioxolanes and 1,3-dioxanes with aliphatic acid chlorides and bromides yields 2- or 3-halohydrine esters. - Keywords: 1,3-Dioxolanes and 1,3-dioxanes, ring opening of

CHARACTER OF THE PRODUCTS OF BROMINATION OF 1,3-DIOXACYCLANES WITH N-BROMOSUCCINIMIDE

The dependence of the character and composition of the products of the reaction of equimolar amounts of N-bromosuccinimide and 1,3-dioxacyclanes on the ring size and the character of the substituent in the 2 position of the 1,3-dioxacyclane ring was examined.Reasons for the primary formation of bromination products of different types for five-, six-, and seven-membered cyclic acetals are proposed.