3,4-dihydro-2H-pyran → HCID 14624889, compound
Reaction equation
[Cl:1][C:2]1[C:7]([OH:8])=[CH:6][C:5]([N:9]=[C:10]=[S:11])=[C:4]([F:12])[CH:3]=1.[O:13]1[CH:18]=[CH:17][CH2:16][CH2:15][CH2:14]1>ClCCl>[Cl:1][C:2]1[C:7]([O:8][CH:14]2[CH2:15][CH2:16][CH2:17][CH2:18][O:13]2)=[CH:6][C:5]([N:9]=[C:10]=[S:11])=[C:4]([F:12])[CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A dichloromethane solution containing 0.10 g of 4-chloro-2-fluoro-5-hydroxyphenylisothiocynate and 0.04 g of 2,3-dihydropyran, was stirred at room temperature for 5 hours. Then, dichloromethane was distilled off, and the residue was washed with diisopropyl ether to obtain 0.11 g of the above-identified compound as white crystals.
Workup
- distillationThen, dichloromethane was distilled off
- washthe residue was washed with diisopropyl ether
Sources & evidence
- ORD record
- ord-3adce5988d4c4ad9b7c43a0b7507c69f
- Source dataset
- uspto-grants-1991_08
- Patent number
- US05039331
Reaction notes
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