2-(2-Chloroethoxy)tetrahydro-2H-pyran → HCID 22116112, compound
Reaction equation
[CH3:1][C:2]1([CH3:13])[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][C:9]=2[CH3:11])[NH:4][C:3]1=[O:12].Cl[CH2:15][CH2:16][O:17]C1CCCCO1>>[OH:17][CH2:16][CH2:15][N:4]1[C:5]2[C:10](=[C:9]([CH3:11])[CH:8]=[CH:7][CH:6]=2)[C:2]([CH3:13])([CH3:1])[C:3]1=[O:12]Participants
3
Procedure
Prepared from 3,3,4-trimethyl-1,3-dihydro-2H-indol-2-one (prepared by the method of Endler and Becker; Organic Syntheses Coll. vol.4, page 657) and 2-(2-chloroethoxy)tetrahydro-2H-pyran as described above.
Workup
- customprepared by the method of Endler and Becker
Sources & evidence
- ORD record
- ord-c16e2489fe9a419898f9bf5e5aa016eb
- Source dataset
- uspto-grants-2000_12
- Patent number
- US06166040
Reaction notes
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