Sodium Cyanide → HCID 15702884, compound
Reaction equation
[C-:1]#[N:2].[Na+].Cl[CH2:5][C:6]1[CH:11]=[CH:10][C:9]([CH2:12][CH2:13][CH2:14][Cl:15])=[CH:8][CH:7]=1>C(O)C>[Cl:15][CH2:14][CH2:13][CH2:12][C:9]1[CH:10]=[CH:11][C:6]([CH2:5][C:1]#[N:2])=[CH:7][CH:8]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In a 100 ml of round bottomed two-necked flask 4.4 g of NaCN, 18.2 g of 1-(4-chloromethylphenyl)3-chloropropane and 44.8 ml of 90% ethanol are added and boiled at reflux for 5 hours. The feedstock is cooled to room temperature and the precipitate is filtered by suction. The filtrate is concentrated by evaporation. The residue is absorbed in 700 ml of diethyl ether, washed to neutrality with 2×250 ml of distilled water and dried with sodium sulfate. The solution is evaporated to dryness in a rotary evaporator.
Workup
- temperatureat reflux for 5 hours
- filtrationthe precipitate is filtered by suction
- concentrationThe filtrate is concentrated by evaporation
- customThe residue is absorbed in 700 ml of diethyl ether
- washwashed
- dry with materialdried with sodium sulfate
- customThe solution is evaporated to dryness in a rotary evaporator
Sources & evidence
- ORD record
- ord-eeb13ca551e64092a22861cab10acadb
- Source dataset
- uspto-grants-1992_06
- Patent number
- US05124326
Reaction notes
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