4-Phenylmercapto-butylbromide → 6-(4-phenylmercapto-butoxy)-4,4-dimethyl-4H-3,1-benzoxazin-2-one
Reaction equation
[OH:1][C:2]1[CH:3]=[CH:4][C:5]2[NH:10][C:9](=[O:11])[O:8][C:7]([CH3:13])([CH3:12])[C:6]=2[CH:14]=1.[C:15]1([S:21][CH2:22][CH2:23][CH2:24][CH2:25]Br)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1>>[C:15]1([S:21][CH2:22][CH2:23][CH2:24][CH2:25][O:1][C:2]2[CH:3]=[CH:4][C:5]3[NH:10][C:9](=[O:11])[O:8][C:7]([CH3:12])([CH3:13])[C:6]=3[CH:14]=2)[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1Participants
3
Procedure
Prepared analogously to Example 5 from 6-hydroxy-4,4-dimethyl-4H-3,1-benzoxazin-2-one and 4-phenylmercaptobutylbromide (B.p. 0.03 mb : 95°-104° C.).
Sources & evidence
- ORD record
- ord-d4096f4aa9524fddb5e68b321000bdd9
- Source dataset
- uspto-grants-1985_05
- Patent number
- US04518597
Reaction notes
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