(R)-5-(4-Chloro-phenyl)-3-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4,5-dihydro-isoxazole

Base Information

Chemical Name:(R)-5-(4-Chloro-phenyl)-3-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4,5-dihydro-isoxazole
CAS No.:178035-83-1
Molecular Formula:C₁₄H₁₆ClNO₃
Molecular Weight:281.739
Hs Code.:

Synonyms:(R)-5-(4-Chloro-phenyl)-3-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4,5-dihydro-isoxazole

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Chemical Property of (R)-5-(4-Chloro-phenyl)-3-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4,5-dihydro-isoxazole

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Technology Process of (R)-5-(4-Chloro-phenyl)-3-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4,5-dihydro-isoxazole

There total 2 articles about (R)-5-(4-Chloro-phenyl)-3-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4,5-dihydro-isoxazole which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 117465-48-2
(S)-2,2-dimethyl-1,3-dioxolane-4-carbaldehyde oxime

: 178035-83-1
(R)-5-(4-Chloro-phenyl)-3-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4,5-dihydro-isoxazole

Guidance literature:: Multi-step reaction with 2 steps

1: N-chlorosuccinimide, pyridine / CHCl₃ / 0.25 h / Ambient temperature

2: Et₃N / CHCl₃ / 16 h / Ambient temperature

With pyridine; N-chloro-succinimide; triethylamine; In chloroform;
DOI:10.1016/0223-5234(96)80366-7

Reference yield:

: 1073-67-2,24991-47-7
4-vinylbenzyl chloride

: C₆H₁₀ClNO₃

: 178035-83-1
(R)-5-(4-Chloro-phenyl)-3-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4,5-dihydro-isoxazole

: 177950-45-7
(S)-5-(4-Chloro-phenyl)-3-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-4,5-dihydro-isoxazole

Guidance literature:: With triethylamine; In chloroform; for 16h; Yield given. Yields of byproduct given; Ambient temperature;
DOI:10.1016/0223-5234(96)80366-7