(1S,2R)-1-phenyl-2-[(S)-1-hydroxypropyl]-N,N-dipropylcyclopropanecarboxamide

Base Information

• Chemical Name: (1S,2R)-1-phenyl-2-[(S)-1-hydroxypropyl]-N,N-dipropylcyclopropanecarboxamide
• CAS No.: 459143-46-5
• Molecular Formula: C₁₉H₂₉NO₂
• Molecular Weight: 303.445
• Mol file: 459143-46-5.mol

Synonyms:(1S,2R)-1-phenyl-2-[(S)-1-hydroxypropyl]-N,N-dipropylcyclopropanecarboxamide

Chemical Property of (1S,2R)-1-phenyl-2-[(S)-1-hydroxypropyl]-N,N-dipropylcyclopropanecarboxamide

Chemical Property:

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

Technology Process of (1S,2R)-1-phenyl-2-[(S)-1-hydroxypropyl]-N,N-dipropylcyclopropanecarboxamide

There total 4 articles about (1S,2R)-1-phenyl-2-[(S)-1-hydroxypropyl]-N,N-dipropylcyclopropanecarboxamide 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: 73.0%

ethylmagnesium bromide (925-90-6) + (1S,2R)-1-phenyl-2-formyl-N,N-dipropylcyclopropanecarboxamide (459143-38-5) → (1S,2R)-1-phenyl-2-[(S)-1-hydroxypropyl]-N,N-dipropylcyclopropanecarboxamide (459143-46-5)

Guidance literature:

In tetrahydrofuran; diethyl ether; at -15 ℃; for 3h;

DOI:10.1016/S0968-0896(02)00030-5

Reference yield:

(1S,5R)-1-phenyl-3-oxabicyclo[3.1.0]hexan-2-one (63106-93-4,96847-52-8,96847-75-5,96847-53-9) → (1S,2R)-1-phenyl-2-[(S)-1-hydroxypropyl]-N,N-dipropylcyclopropanecarboxamide (459143-46-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 84 percent / AlCl₃ / CH₂Cl₂ / 24 h / 20 °C

2: 94 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -78 °C

3: 73 percent / tetrahydrofuran; diethyl ether / 3 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)00030-5

Reference yield:

di-n-propylamine (142-84-7) → (1S,2R)-1-phenyl-2-[(S)-1-hydroxypropyl]-N,N-dipropylcyclopropanecarboxamide (459143-46-5)

Guidance literature:

Multi-step reaction with 3 steps

1: 84 percent / AlCl₃ / CH₂Cl₂ / 24 h / 20 °C

2: 94 percent / (COCl)2; DMSO; Et₃N / CH₂Cl₂ / -78 °C

3: 73 percent / tetrahydrofuran; diethyl ether / 3 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)00030-5

upstream raw materials:

ethylmagnesium bromide

(1S,2R)-1-phenyl-2-formyl-N,N-dipropylcyclopropanecarboxamide

(1S,5R)-1-phenyl-3-oxabicyclo[3.1.0]hexan-2-one

di-n-propylamine

Downstream raw materials:

(1S,2R)-1-phenyl-2-[(S)-1-azidopropyl]-N,N-dipropylcyclopropanecarboxamide

(1S,4S,5R)-2-oxo-4-ethyl-1-phenyl-3-oxabicyclo[3.1.0]hexane