Ether hydrochloride → HCID 85707177, compound
Reaction equation
[CH3:1][N:2]([CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[Te:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1)[CH3:3].[ClH:18].CCOCC>CCOCC.C(O)(C)C>[ClH:18].[CH3:1][N:2]([CH3:3])[CH2:4][C:5]1[CH:10]=[CH:9][CH:8]=[CH:7][C:6]=1[Te:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To a slurry of 2-(N,N-dimethylaminomethyl)-1-phenyltellurobenzene (1.02 g, 3.0 mmol) in ether (50 mL) in a water bath was added dropwise by syringe a hydrogen chloride/ether solution (3.15 mL, 1.0 M, 3.15 mmol). The thick slurry was diluted with isopropanol (20 mL) then filtered. The white solid was washed with ether, and air dried, to give the product (1.13 g, 95%). 1H NMR (CDCl3) d 2.6 (1H, br s), 8.13 (1H, d, J=7.5), 7.80 (1H, d, J=7.7), 7.52-7.48 (3H, m), 7.26-7.17 (4H, m), 4.44 (2H, d, J=5.8), 2.68 (6H, d, J=4.5). Anal. calc'd for C15H18ClNTe: C, 48.00; H, 4.83; N, 3.73. Found: C, 47.97; H, 4.87; N, 3.65.
Workup
- filtrationthen filtered
- washThe white solid was washed with ether, and air
- customdried
Sources & evidence
- ORD record
- ord-50e02106c9ac492eaec25a4b3c741098
- Source dataset
- uspto-grants-1999_07
- Patent number
- US05928886
Reaction notes
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