Formaldehyde → HCID 70926255, compound
Reaction equation
C([C:4]1[C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH:7]=[CH:6][CH:5]=1)(=O)C.[NH2:14][CH2:15][CH2:16][CH2:17][CH2:18][NH:19][CH2:20][CH2:21][CH2:22][NH2:23].[CH2:24]=O.O1[CH2:31][CH2:30][O:29]CC1>>[NH2:23][CH2:22][CH2:21][CH2:20][NH:19][CH2:18][CH2:17][CH2:16][CH2:15][NH:14][CH2:24][CH2:31][C:30]([C:6]1[CH:5]=[CH:4][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH:7]=1)=[O:29]Participants
5
Procedure
Acetyl naphthalene (170 mg), spermidine (145 mg), and paraformaldehyde (36 mg) were reacted in dioxane (0.2 ml) at 150° C. for 2 hours.
Sources & evidence
- ORD record
- ord-2a15a111190b4469a5e3a04ffd4e00ee
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08937091B2
Reaction notes
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