Hydrochloric Acid → HCID 138413, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][CH:8]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)O)[CH:2]=1.Cl>C(O)(=O)C>[N:1]1[CH:6]=[CH:5][CH:4]=[C:3]([CH:7]=[CH:8][C:10]2[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=2)[CH:2]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of crude 2-(3-pyridyl)-1-phenylethanol (20 g), glacial acetic acid (200 ml) and concentrated HCl (50 ml) is refluxed for 16 hours, then evaporated to dryness in vacuo. The oily hydrochloride is taken up in water, extracted with ether and methylene chloride, and then liberated with bicarbonate. Extraction (CH2Cl2) and drying (K2CO3) affords 13 g of β-(3-pyridyl)styrene.
Workup
- temperatureis refluxed for 16 hours
- customevaporated to dryness in vacuo
- extractionextracted with ether and methylene chloride
- extractionExtraction (CH2Cl2)
- dry with materialdrying (K2CO3)
Sources & evidence
- ORD record
- ord-dcdf81f575f14605b562cd3fe9157e7a
- Source dataset
- uspto-grants-1976_04
- Patent number
- US03953434
Reaction notes
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