Triethyl phosphite → HCID 67777907, compound
Reaction equation
[CH:1]1([CH2:4][O:5][C:6]2[CH:11]=[CH:10][C:9]([N:12]=[N:13][C:14]3[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][CH:15]=3)=[C:8]([N+:21]([O-])=O)[CH:7]=2)[CH2:3][CH2:2]1.P(OCC)(OCC)OCC>>[CH:1]1([CH2:4][O:5][C:6]2[CH:11]=[CH:10][C:9]3=[N:12][N:13]([C:14]4[CH:19]=[CH:18][C:17]([OH:20])=[CH:16][CH:15]=4)[N:21]=[C:8]3[CH:7]=2)[CH2:3][CH2:2]1Participants
3
Conditions
- Temperature
- 140 °C
Procedure
A mixture of 4-{[4-(cyclopropylmethoxy)-2-nitrophenyl]diazenyl}phenol and triethyl phosphite (4 mL) was stirred at 140° C. overnight. The reaction mixture was purified by silica gel column chromatography (hexane/ethyl acetate) to give the title compound as a yellow solid (103 mg).
Workup
- customThe reaction mixture was purified by silica gel column chromatography (hexane/ethyl acetate)
Sources & evidence
- ORD record
- ord-705e89c5c32d4f2f9201dbe36ceaa156
- Source dataset
- uspto-grants-2014_05
- Patent number
- US08729102B2
Reaction notes
Loading…