3-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one

Base Information

Chemical Name:3-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one
CAS No.:1394249-59-2
Molecular Formula:C₁₈H₂₁NO₂
Molecular Weight:283.37
Hs Code.:

Synonyms:3-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one

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Chemical Property of 3-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one

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Technology Process of 3-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one

There total 2 articles about 3-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one 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: 64.0%

: 37580-42-0
(E)-2-methyl-1-phenyl-1,3-butadiene

: 3-(buta-1,2-dien-1-yl)oxazolidin-2-one

: 1394249-59-2
3-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one

Guidance literature:: With silver hexafluoroantimonate; C₃₁H₂₉AuClN₃; In dichloromethane; at -50 ℃; for 16h; enantioselective reaction; Molecular sieve;
DOI:10.1021/ja3065446

Reference yield:

: 37580-42-0
(E)-2-methyl-1-phenyl-1,3-butadiene

: 3-(buta-1,2-dien-1-yl)oxazolidin-2-one

: 1394249-59-2
3-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one

: 1394249-60-5
3-{(Z)-[(2S,6R)-3,6-dimethyl-2-phenylcyclohex-3-en-1-ylidene]methyl}-1,3-oxazolidin-2-one

Guidance literature:: With C₃₆H₃₇AuClN₃; silver(I) triflimide; In dichloromethane; at -50 - -15 ℃; for 2h; Overall yield = 75 %; enantioselective reaction; Molecular sieve;
DOI:10.1021/ja3065446