تفاعل #2465
ord-d7d6fec5e6d54cc5b295691760de5f99
معادلة التفاعل
ammonia
acetate
( ii )
1-(2-acetoxypropionyl)-1,2,3,4-tetrahydro-2,2,4-trimethylquinoline
H2SO4
→
desired product
المردود 75.0%
4-amino-1,1,3-trimethylindane
المردود 75.0%
المتفاعلات
الكواشف
لا شيء
المذيبات
ظروف التفاعل
درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1workup.ADDITIONwas cautiously added dropwise
- 2درجة الحرارةthe mixture heated at 100° C. for 3 hours
- 3أخرىSeparation of the organic layer
- 4تجفيفdrying (MgSO4) and solvent flash
الإجراء التجريبي
The acetate compound prepared in B (ii) (55 g, GC purity 91%, 0.172 moles) was added over 45 minutes to 98% H2SO4 (50 ml) at 25°-60° C. (exotherm). After stirring for a further 30 minutes at 60° C., water (50 ml) containing acetic acid (10 ml) was cautiously added dropwise and the mixture heated at 100° C. for 3 hours. Petrol (60/80 b.p., 100 ml) was added and the mixture basified to pH 9 with 35% aqueous ammonia (150 ml). Separation of the organic layer, drying (MgSO4) and solvent flash gave the desired product (22.6 g, GC purity 92%, yield 69%). NMR analysis using chiral solvating agent [(-)-2,2,2-trifluoro-1-(9-anthryl)ethanol] showed a 70/30 mixture of enantiomers in favour of the (-)-isomer.