Hydrochloric Acid → HCID 13364595, compound
Reaction equation
OC1C=C(OC(CCCC2C=CC=CC=2)C)C=C2C=1C(C(OC1C=CC([N+]([O-])=O)=CC=1)=O)CC(C)(C)C2.CN.Cl.C[NH-].C[NH:44][C:45]([CH:47]1[C:56]2[C:51](=[CH:52][C:53]([O:58][CH:59]([CH2:61][CH2:62][CH2:63][C:64]3[CH:69]=[CH:68][CH:67]=[CH:66][CH:65]=3)[CH3:60])=[CH:54][C:55]=2[OH:57])[CH2:50][C:49]([CH3:71])([CH3:70])[CH2:48]1)=[O:46]>O1CCCC1>[OH:57][C:55]1[CH:54]=[C:53]([O:58][CH:59]([CH2:61][CH2:62][CH2:63][C:64]2[CH:65]=[CH:66][CH:67]=[CH:68][CH:69]=2)[CH3:60])[CH:52]=[C:51]2[C:56]=1[CH:47]([C:45]([NH2:44])=[O:46])[CH2:48][C:49]([CH3:71])([CH3:70])[CH2:50]2Participants
7
Procedure
Reaction of 0.55 g. (1.1 mmole) p-nitrophenyl 8-hydroxy-3,3-dimethyl-6-(5-phenyl-2-pentyloxy)tetralin-1-carboxylate in 10 ml. tetrahydrofuran with an excess of methylamine (gas) at room temperature, pouring the resulting mixture into 10% hydrochloric acid, extracting with ethyl acetate and work-up in the usual manner affords 0.50 g. of the N-methyl amide: N-methyl 8-hydroxy-3,3-dimethyl-6-(5-phenyl-2-pentyloxy)tetralin-1-carboxamide as a foam. 1H-NMR (CDCl3) ppm (delta): 0.8 (s, 3H), 1.0 (s, 3H), 1.2 (d, 4H), 1.7 (m, 6H), 2.53 (m, 6H), 3.6 (m, 1H), 4.23 (m, NH), 6.2 (d, 2H), 7.13 (s, 5H).
Workup
- customReaction of 0.55 g
- extractionextracting with ethyl acetate
- customaffords 0.50 g
Sources & evidence
- ORD record
- ord-f2cf460af9694bdd8260d9e18861ce31
- Source dataset
- uspto-grants-1989_09
- Patent number
- US04863934
Reaction notes
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