(+)-(3R,4E,S(S))-4-(p-tolylsulfinyl)non-4-en-3-yl 2,2,2-trichloroacetimidate

Base Information

Chemical Name:(+)-(3R,4E,S(S))-4-(p-tolylsulfinyl)non-4-en-3-yl 2,2,2-trichloroacetimidate
CAS No.:1380096-55-8
Molecular Formula:C₁₈H₂₄Cl₃NO₂S
Molecular Weight:424.819
Hs Code.:

Synonyms:(+)-(3R,4E,S(S))-4-(p-tolylsulfinyl)non-4-en-3-yl 2,2,2-trichloroacetimidate

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of (+)-(3R,4E,S(S))-4-(p-tolylsulfinyl)non-4-en-3-yl 2,2,2-trichloroacetimidate

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Technology Process of (+)-(3R,4E,S(S))-4-(p-tolylsulfinyl)non-4-en-3-yl 2,2,2-trichloroacetimidate

There total 1 articles about (+)-(3R,4E,S(S))-4-(p-tolylsulfinyl)non-4-en-3-yl 2,2,2-trichloroacetimidate 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: 95.0%

: 131973-93-8,131973-90-5
(E)-4(S_S)-(p-tolylsulfinyl)pent-4-en-3(R)-ol

: 545-06-2
trichloroacetonitrile

: 1380096-55-8
(+)-(3R,4E,S(S))-4-(p-tolylsulfinyl)non-4-en-3-yl 2,2,2-trichloroacetimidate

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In acetonitrile; at 0 - 20 ℃; for 0.25h; Inert atmosphere;
DOI:10.1021/ol301139a

Reference yield:

: 1380096-55-8
(+)-(3R,4E,S(S))-4-(p-tolylsulfinyl)non-4-en-3-yl 2,2,2-trichloroacetimidate

: 1380096-91-2
2,2,2-trichloro-N-((5S,3E,S(S))-4-(p-tolylsulfinyl)non-3-en-5-yl)acetamide

: 1380096-81-0
(-)-2,2,2-trichloro-N-((5R,3Z,S(S))-4-(p-tolylsulfinyl)non-3-en-5-yl)acetamide

Guidance literature:: With 2,6-di-tert-butyl-4-methyl-phenol; In N,N-dimethyl-formamide; at 100 ℃; for 24h; optical yield given as %de; diastereoselective reaction; Inert atmosphere;
DOI:10.1021/ol301139a