Reaction equation
Cl.[C:2]([NH:6][NH2:7])([CH3:5])([CH3:4])[CH3:3].[C:8]1(=[O:27])[C:21]2[C:22]3=[C:23]4[C:18](=[CH:19][CH:20]=2)[CH:17]=[CH:16][CH:15]=[C:14]4[CH:13]=[CH:12][C:11]3=[CH:10][CH:9]1[C:24](Cl)=[O:25].CC[O:30][CH2:31][CH3:32].CCCCCC.[C:39]1([CH3:45])[CH:44]=C[CH:42]=[CH:41][CH:40]=1>[OH-]>[C:2]([N:6]([C:31]([C:32]1[CH:44]=[C:39]([CH3:45])[CH:40]=[CH:41][CH:42]=1)=[O:30])[NH:7][C:24]([CH:9]1[CH:10]=[C:11]2[C:22]3=[C:23]4[C:18]([CH:17]=[CH:16][CH:15]=[C:14]4[CH:13]=[CH:12]2)=[CH:19][CH:20]=[C:21]3[C:8]1=[O:27])=[O:25])([CH3:5])([CH3:4])[CH3:3]Participants
7
Procedure
To a stirred suspension of t-butyl hydrazine hydrochloride (0.02 mol) in toluene (20 ml) and aqueous hydroxide (5 ml of 50% solution) at room temperature was added pyrenonecarbonyl chloride (0.01 mol). After stirring the reaction mixture for 20 minutes, ether and hexane were added and the solid product was filtered and washed with water. The solid product (0.5 g) was stirred in toluene (10 ml) and aqueous sodium hydroxide and m-toluoyl chloride (0.8 g) was added dropwise. After stirring for 5 hours, hexane and ether were added and the solid product filtered and air dried.
Workup
- filtrationthe solid product was filtered
- washwashed with water
- stirringThe solid product (0.5 g) was stirred in toluene (10 ml)
- additionaqueous sodium hydroxide and m-toluoyl chloride (0.8 g) was added dropwise
- stirringAfter stirring for 5 hours
- additionhexane and ether were added
- filtrationthe solid product filtered
- customair dried
Sources & evidence
- ORD record
- ord-4ace12a6e29447b3bbd6b021605bd28a
- Source dataset
- uspto-grants-1995_06
- Patent number
- US05424333
Linked notes
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