تفاعل #2465

ord-d7d6fec5e6d54cc5b295691760de5f99

معادلة التفاعل

N
ammonia
CC(=O)[O-]
acetate
CC(=O)OC(C)C(=O)N1c2ccccc2C(C)CC1(C)C
( ii )
CC(=O)OC(C)C(=O)N1c2ccccc2C(C)CC1(C)C
1-(2-acetoxypropionyl)-1,2,3,4-tetrahydro-2,2,4-trimethylquinoline
O=S(=O)(O)O
H2SO4
CC1CC(C)(C)c2cccc(N)c21
desired product
المردود 75.0%
CC1CC(C)(C)c2cccc(N)c21
4-amino-1,1,3-trimethylindane
المردود 75.0%

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas cautiously added dropwise
  2. 2
    درجة الحرارةthe mixture heated at 100° C. for 3 hours
  3. 3
    أخرىSeparation of the organic layer
  4. 4
    تجفيفdrying (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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05728869uspto-grants-1998_03