2-(1-Chloroethyl)pyridine

Base Information

• Chemical Name: 2-(1-Chloroethyl)pyridine
• CAS No.: 10445-92-8
• Molecular Formula: C7H8 Cl N
• Molecular Weight: 141.6
• Hs Code.: 2933399090
• DSSTox Substance ID: DTXSID20506498
• Nikkaji Number: J980.701B
• Mol file: 10445-92-8.mol

Synonyms:2-(1-Chloroethyl)pyridine;10445-92-8;2-(1-Chloro-ethyl)-pyridine;Pyridine, 2-(1-chloroethyl)-;Pyridine, 2-(1-chloroethyl)- (7CI,8CI,9CI);2-(1-chloroethyl)-pyridine;2-(1-Chloro-ethyl)pyridine;SCHEMBL678429;DTXSID20506498;ZHBVIIQZRLPHGH-UHFFFAOYSA-N;MFCD10690742;AKOS009237891;AM90521;SB30356;FT-0755410;F13293;A896227

Chemical Property of 2-(1-Chloroethyl)pyridine

Chemical Property:

• Boiling Point: 192oC
• Flash Point: 87oC
• PSA: 12.89000
• Density: 1.109
• LogP: 2.38140
• Storage Temp.: 2-8°C
• XLogP3: 1.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 141.0345270
• Heavy Atom Count: 9
• Complexity: 85

Purity/Quality:

N≥12% ^*data from raw suppliers

2-(1-Chloroethyl)pyridine ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(C1=CC=CC=N1)Cl

Technology Process of 2-(1-Chloroethyl)pyridine

There total 7 articles about 2-(1-Chloroethyl)pyridine 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: 70.0%

2-chloromethylpyridine (4377-33-7) + methyl iodide (74-88-4) → 2-(1-chloroethyl)pyridine (10445-92-8)

Guidance literature:

With lithium diisopropyl amide; In tetrahydrofuran; at -78 ℃; for 1h;

DOI:10.1016/S0040-4039(00)76860-2

Reference yield: 48.0%

2-ethylpyridine 1-oxide (4833-24-3) + 4-chloro-2,2-dimethyl-2H-benzo[e][1,3]oxazine (74405-07-5) → 2,2-dimethyl-4-keto-1,3-benzoxazine (30914-88-6) + 2-(1-chloroethyl)pyridine (10445-92-8) + 3-(6-Ethyl-pyridin-2-yl)-2,2-dimethyl-2,3-dihydro-benzo[e][1,3]oxazin-4-one (76809-22-8) + 2,2-Dimethyl-3-(1-pyridin-2-yl-ethyl)-2,3-dihydro-benzo[e][1,3]oxazin-4-one (76809-15-9) + 3-(6-Ethyl-pyridin-3-yl)-2,2-dimethyl-2,3-dihydro-benzo[e][1,3]oxazin-4-one; hydrochloride (76809-32-0) + 3-(2-Ethyl-pyridin-3-yl)-2,2-dimethyl-2,3-dihydro-benzo[e][1,3]oxazin-4-one; hydrochloride (76809-25-1)

Guidance literature:

In 1,2-dichloro-ethane; for 2h; Mechanism; Product distribution; Heating;

Reference yield: 25.0%

2-Ethylpyridine (100-71-0) → 2-(1-chloroethyl)pyridine (10445-92-8)

Guidance literature:

With trichloroisocyanuric acid; In 1,2-dichloro-ethane; for 2h; Heating;

upstream raw materials:

2-Ethylpyridine

2-chloromethylpyridine

methyl iodide

2-ethylpyridine 1-oxide

Downstream raw materials:

2-acetylpyridine

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