(1S,2R)-1-(2-fluorophenyl)-2-[(S)-1-hydroxypropyl]-N,N-diethylcyclopropanecarboxamide

Base Information

Chemical Name:(1S,2R)-1-(2-fluorophenyl)-2-[(S)-1-hydroxypropyl]-N,N-diethylcyclopropanecarboxamide
CAS No.:528587-93-1
Molecular Formula:C₁₇H₂₄FNO₂
Molecular Weight:293.381
Hs Code.:

Synonyms:(1S,2R)-1-(2-fluorophenyl)-2-[(S)-1-hydroxypropyl]-N,N-diethylcyclopropanecarboxamide

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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)-1-(2-fluorophenyl)-2-[(S)-1-hydroxypropyl]-N,N-diethylcyclopropanecarboxamide

Chemical Property:

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Technology Process of (1S,2R)-1-(2-fluorophenyl)-2-[(S)-1-hydroxypropyl]-N,N-diethylcyclopropanecarboxamide

There total 4 articles about (1S,2R)-1-(2-fluorophenyl)-2-[(S)-1-hydroxypropyl]-N,N-diethylcyclopropanecarboxamide 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: 77.0%

: 925-90-6
ethylmagnesium bromide

: 528587-85-1
(1S,2R)-1-(2-fluorophenyl)-2-formyl-N,N-diethylcyclopropanecarboxamide

: 528587-93-1
(1S,2R)-1-(2-fluorophenyl)-2-[(S)-1-hydroxypropyl]-N,N-diethylcyclopropanecarboxamide

Guidance literature:: In tetrahydrofuran; diethyl ether; at -15 ℃; for 4h;
DOI:10.1016/S0968-0896(02)00346-2

Reference yield:

: 326-62-5
2-fluorophenyl acetonitrile

: 528587-93-1
(1S,2R)-1-(2-fluorophenyl)-2-[(S)-1-hydroxypropyl]-N,N-diethylcyclopropanecarboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: NaNH₂ / benzene / 2 h / 20 °C

1.2: 28 percent / benzene / 2 h / 20 °C

2.1: 100 percent / AlCl₃ / CH₂Cl₂ / 18 h / 20 °C

3.1: 87 percent / oxalyl chloride; DMSO; Et₃N / CH₂Cl₂ / 2.5 h / -78 °C

4.1: 77 percent / diethyl ether; tetrahydrofuran / 4 h / -15 °C

With aluminium trichloride; oxalyl dichloride; sodium amide; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; diethyl ether; dichloromethane; benzene; 3.1: Swern oxidation / 4.1: Grignard reaction;
DOI:10.1016/S0968-0896(02)00346-2

Reference yield:

: 528587-69-1
(1S,5R)-2-oxo-1-(2-fluorophenyl)-3-oxabicyclo[3.1.0]hexane

: 528587-93-1
(1S,2R)-1-(2-fluorophenyl)-2-[(S)-1-hydroxypropyl]-N,N-diethylcyclopropanecarboxamide

Guidance literature:: Multi-step reaction with 3 steps

1: 100 percent / AlCl₃ / CH₂Cl₂ / 18 h / 20 °C

2: 87 percent / oxalyl chloride; DMSO; Et₃N / CH₂Cl₂ / 2.5 h / -78 °C

3: 77 percent / diethyl ether; tetrahydrofuran / 4 h / -15 °C

With aluminium trichloride; oxalyl dichloride; dimethyl sulfoxide; triethylamine; In tetrahydrofuran; diethyl ether; dichloromethane; 2: Swern oxidation / 3: Grignard reaction;
DOI:10.1016/S0968-0896(02)00346-2