تفاعل #54756

ord-c5f2f03608c945db9b80e903cc970a15

معادلة التفاعل

CC(C)=CCBr
3,3-Dimethylallyl bromide
COc1cccc([C@@]23CCCC[C@H]2C(=O)NC(=O)C3)c1
4a-(m-methoxyphenyl)-1,3-diketo-trans-decahydroisoquinoline
[H-].[Na+]
sodium hydride
O
water
COc1cccc([C@@]23CCCC[C@@H]2C(=O)N(CC=C(C)C)C(=O)C3)c1
N-(3,3-dimethylallyl)-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline
المردود 94.4%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction mixture was heated for 1 hour
  2. 2
    workup.ADDITIONafter the addition
  3. 3
    درجة الحرارةcooled to 25°
  4. 4
    درجة الحرارةAfter heating at 80° for 1 hour it
  5. 5
    استخلاصextracted with ether

الإجراء التجريبي

A solution of 4 g (14.7 mmoles) of 4a-(m-methoxyphenyl)-1,3-diketo-trans-decahydroisoquinoline in 50 ml of anhydrous dimethylformamide was added dropwise to 700 mg of a 55% suspension of sodium hydride in mineral oil in 50 ml of dimethylformamide at 70°. The reaction mixture was heated for 1 hour after the addition was complete and then cooled to 25°. 3,3-Dimethylallyl bromide (2.37 g, 15.8 mmoles) in 10 ml of dimethylformamide was added dropwise and the solution stirred overnight at 25°. After heating at 80° for 1 hour it was poured into water and extracted with ether to yield 4.74 g of N-(3,3-dimethylallyl)-4a-(m-methoxyphenyl)-1,3-diketo-cis-decahydroisoquinoline (oil), which was evaporatively distilled, bp 225° (0.005 mm).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04150135uspto-grants-1979_04