Hydrochloric Acid → HCID 20324112, compound
Reaction equation
[C:1]([CH2:3][C:4]1[CH:9]=[CH:8][C:7]([NH:10][C:11](=[O:20])[O:12][CH2:13][C:14]2[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=2)=[CH:6][CH:5]=1)#[N:2].[ClH:21]>CC(C)=O>[ClH:21].[C:1]([CH2:3][C:4]1[CH:9]=[CH:8][C:7]([NH:10][C:11](=[O:20])[O:12][CH2:13][C:14]2[CH:15]=[N:16][CH:17]=[CH:18][CH:19]=2)=[CH:6][CH:5]=1)#[N:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 3-pyridylmethyl N-(4-cyanomethylphenyl)carbamate (5 g., 0.0187 mole) in 300 ml. of acetone was added an excess of hydrogen chloride in a steady stream. A white suspension formed and was filtered off to give 5.3 g. of solid melting at 215°-216° C. This was a 93.5% yield of 3-pyridylmethyl N-(4-cyanomethylphenyl)carbamate hydrochloride.
Workup
- customA white suspension formed
- filtrationwas filtered off
- customto give 5.3 g
Sources & evidence
- ORD record
- ord-5bd734d5866e446389b7b0248ae3319a
- Source dataset
- uspto-grants-1978_06
- Patent number
- US04094875
Reaction notes
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