(6S)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-6H-1,2-oxazine

Base Information

Chemical Name:(6S)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-6H-1,2-oxazine
CAS No.:205764-47-2
Molecular Formula:C₂₀H₂₇NO₂
Molecular Weight:313.44
Hs Code.:

Synonyms:(6S)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-6H-1,2-oxazine

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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 (6S)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-6H-1,2-oxazine

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Technology Process of (6S)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-6H-1,2-oxazine

There total 1 articles about (6S)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-6H-1,2-oxazine 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: 28.0%

: 2216-51-5
(-)-menthol

: 165554-70-1
6-ethoxy-3-phenyl-6H-1,2-oxazine

: 205764-47-2
(6S)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-6H-1,2-oxazine

: 491838-92-7
(6R)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-6H-1,2-oxazine

Guidance literature:: With boron trifluoride diethyl etherate; In dichloromethane; at 20 ℃; for 24h;
DOI:10.1002/1099-0690(200208)2002:16<2838::AID-EJOC2838>3.0.CO;2-O

Reference yield: 94.0%

: 205764-47-2
(6S)-[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyloxy]-3-phenyl-6H-1,2-oxazine

: (4S,5S,6S)-6-[(1'R,2'S,5'R)-2'-isopropyl-5'-methylcyclohexyloxy]-4,5-epoxy-3-phenyl-5,6-dihydro-4H-1,2-oxazine

Guidance literature:: With tert.-butylhydroperoxide; potassium fluoride on basic alumina; In decane; acetonitrile; at 20 ℃; for 24h; diastereoselective reaction; Inert atmosphere;
DOI:10.1002/ejoc.201000425