(1S,2R)-N-<(R)-2-hydroxy-1-phenylethyl>-2-(2-methoxyphenyl)cyclopropanecarboxamide

Base Information

Chemical Name:(1S,2R)-N-<(R)-2-hydroxy-1-phenylethyl>-2-(2-methoxyphenyl)cyclopropanecarboxamide
CAS No.:110901-79-6
Molecular Formula:C₁₉H₂₁NO₃
Molecular Weight:311.381
Hs Code.:

Synonyms:(1S,2R)-N-<(R)-2-hydroxy-1-phenylethyl>-2-(2-methoxyphenyl)cyclopropanecarboxamide

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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 (1S,2R)-N-<(R)-2-hydroxy-1-phenylethyl>-2-(2-methoxyphenyl)cyclopropanecarboxamide

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Technology Process of (1S,2R)-N-<(R)-2-hydroxy-1-phenylethyl>-2-(2-methoxyphenyl)cyclopropanecarboxamide

There total 6 articles about (1S,2R)-N-<(R)-2-hydroxy-1-phenylethyl>-2-(2-methoxyphenyl)cyclopropanecarboxamide 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: 44.0%

: 56613-80-0
D-2-phenylglycinol

: 110826-43-2
(1R,2R)-2-(2-Methoxy-phenyl)-cyclopropanecarbonyl chloride

: 110901-79-6
(1S,2R)-N-<(R)-2-hydroxy-1-phenylethyl>-2-(2-methoxyphenyl)cyclopropanecarboxamide

: 110826-31-8
(1R,2S)-N-<(R)-2-hydroxy-1-phenylethyl>-2-(2-methoxyphenyl)cyclopropanecarboxamide

Guidance literature:: With triethylamine; In dichloromethane; 1.) 0 deh C, 30 min, 2.) room temperature, overnight;
DOI:10.1021/jm00396a014

Reference yield:

: 1011-54-7
2-methoxycinnamic acid

: 110901-79-6
(1S,2R)-N-<(R)-2-hydroxy-1-phenylethyl>-2-(2-methoxyphenyl)cyclopropanecarboxamide

Guidance literature:: Multi-step reaction with 5 steps

2: 100 percent / Pd(OAc)2 / diethyl ether; CH₂Cl₂ / 1 h / -10 - -5 °C

3: 92 percent / NaOH / methanol

4: SOCl₂ / 0.75 h / 55 °C

5: 43 percent / Et₃N / CH₂Cl₂ / 1.) 0 deh C, 30 min, 2.) room temperature, overnight

With sodium hydroxide; thionyl chloride; triethylamine; palladium diacetate; In methanol; diethyl ether; dichloromethane;
DOI:10.1021/jm00396a014

Reference yield:

: 98288-15-4
methyl 2-methoxycinnamate

: 110901-79-6
(1S,2R)-N-<(R)-2-hydroxy-1-phenylethyl>-2-(2-methoxyphenyl)cyclopropanecarboxamide

Guidance literature:: Multi-step reaction with 4 steps

1: 100 percent / Pd(OAc)2 / diethyl ether; CH₂Cl₂ / 1 h / -10 - -5 °C

2: 92 percent / NaOH / methanol

3: SOCl₂ / 0.75 h / 55 °C

4: 43 percent / Et₃N / CH₂Cl₂ / 1.) 0 deh C, 30 min, 2.) room temperature, overnight

With sodium hydroxide; thionyl chloride; triethylamine; palladium diacetate; In methanol; diethyl ether; dichloromethane;
DOI:10.1021/jm00396a014