3-Bromo-4-(3-hydroxypropyl)pyridine

Base Information

• Chemical Name: 3-Bromo-4-(3-hydroxypropyl)pyridine
• CAS No.: 229184-01-4
• Molecular Formula: C8H10BrNO
• Molecular Weight: 216.07500
• DSSTox Substance ID: DTXSID00472864
• Wikidata: Q82302050
• Mol file: 229184-01-4.mol

Synonyms:229184-01-4;3-Bromo-4-(3-hydroxypropyl)pyridine;3-(3-bromopyridin-4-yl)propan-1-ol;4-Pyridinepropanol, 3-bromo-;SCHEMBL2654216;DTXSID00472864;UFMZEYFJEDBAGO-UHFFFAOYSA-N;3-(3-bromopyridin-4-yl)-1-propanol;FT-0729875;EN300-1626917

Chemical Property of 3-Bromo-4-(3-hydroxypropyl)pyridine

Chemical Property:

• PSA: 33.12000
• LogP: 1.76900
• XLogP3: 1.5
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 214.99458
• Heavy Atom Count: 11
• Complexity: 110

Purity/Quality:

95% ^*data from raw suppliers

3-BROMO-4-(3-HYDROXYPROPYL)PYRIDINE 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CN=CC(=C1CCCO)Br

Technology Process of 3-Bromo-4-(3-hydroxypropyl)pyridine

There total 1 articles about 3-Bromo-4-(3-hydroxypropyl)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: 78.0%

oxirane (75-21-8,99932-75-9) + 3-Bromo-4-methylpyridin (3430-22-6) → 3-bromo-4-[3-hydroxypropyl]pyridine (229184-01-4)

Guidance literature:

With lithium diisopropyl amide; at -20 ℃;

DOI:10.1016/j.bmcl.2004.01.057

Reference yield: 33.0%

3-bromo-4-[3-hydroxypropyl]pyridine (229184-01-4) + 5-benzyloxy-3-(4-methyl-thiazol-2-yl)-1H-pyridin-2-one (216011-87-9) → 5-benzyloxy-1-[3-(3-bromo-pyridin-4-yl)-propyl]-3-(4-methyl-thiazol-2-yl)-1H-pyridin-2-one (216012-90-7)

Guidance literature:

With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 0 - 25 ℃; for 1h;

DOI:10.1016/S0040-4039(99)00652-8

Reference yield:

3-bromo-4-[3-hydroxypropyl]pyridine (229184-01-4) → 1-{4-[3-(tert-butyldimethylsilanyloxy)propyl]pyridin-3-yl}-2-o-tolylethanone (489466-58-2)

Guidance literature:

Multi-step reaction with 6 steps

1: 100 percent / imidazole / CH₂Cl₂ / 17 h / 20 °C

2: 88 percent / N-ethyldiisopropylamine; 1,3-bis(diphenylphosphino)propane / palladium(II) acetate / dimethylformamide / 20 h / 20 - 95 °C

3: 89 percent / potassium trimethylsilanolate / diethyl ether / 48 h / 20 °C

4: dimethylformamide / 1.5 h / 50 °C

5: 1.69 g / 60percent sodium hydride / dimethylformamide / 3.25 h / -10 - 20 °C

6: 76 percent / sodium chloride; water / dimethylsulfoxide / 0.5 h / 150 °C

With 1H-imidazole; 1,3-bis-(diphenylphosphino)propane; potassium trimethylsilonate; water; N-ethyl-N,N-diisopropylamine; sodium chloride; palladium diacetate; In diethyl ether; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; 5: Claisen condensation;

DOI:10.1021/jo026411a

upstream raw materials:

oxirane

3-Bromo-4-methylpyridin

Downstream raw materials:

5-benzyloxy-1-[3-(3-bromo-pyridin-4-yl)-propyl]-3-(4-methyl-thiazol-2-yl)-1H-pyridin-2-one

1-{4-[3-(tert-butyldimethylsilanyloxy)propyl]pyridin-3-yl}-3-(dimethylamino)-2-phenylpropenone

1-{4-[3-(tert-butyldimethylsilanyloxy)propyl]pyridin-3-yl}-3-(dimethylamino)-2-o-tolylpropenone

1-{4-[3-(tert-butyldimethylsilanyloxy)propyl]pyridin-3-yl}-2-phenylethanone