تفاعل #84032

ord-ac829fdf154e4a9aaa5812f622a5b372

معادلة التفاعل

CON(C)C(=O)c1ccc2cc(Br)ccc2c1
6-bromo-N-methoxy-N-methyl-2-naphthamide
[CH3][Mg][Br]
methyl magnesium bromide
Cl
hydrochloric acid
CC(=O)c1ccc2cc(Br)ccc2c1
1-(6-bromonaphthalen-2-yl)-ethanone
المردود 99.0%

المذيبات

ظروف التفاعل

درجة الحرارة
12.5°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction mixture was cooled in an ice bath
  2. 2
    درجة الحرارةcarefully added drop wise while cooling on an ice bath
  3. 3
    أخرىThe organic solvent was evaporated
  4. 4
    استخلاصthe precipitated product extracted with dichloromethane (500 mL)
  5. 5
    تجفيفThe solution was dried over sodium sulphate
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated
  8. 8
    أخرىThe solid residue was dried in vacuum at 40° C.

الإجراء التجريبي

6-bromo-N-methoxy-N-methyl-2-naphthamide (82.9 g, 282 mmol, 1 equiv.) was dissolved in tetrahydrofurane (600 mL) in a 4-neck flask under nitrogen. The reaction mixture was cooled in an ice bath and methyl magnesium bromide (3.2 M in methyl-tetrahydrofurane, 197 mL, 2.2 equiv.) was added drop wise during 1 hour, while maintaining the temperature of the reaction mixture between 10-15° C. The reaction mixture was stirred 30 minutes further in an ice bath. Aqueous hydrochloric acid (2 M, 100 mL) was then carefully added drop wise while cooling on an ice bath. The organic solvent was evaporated and the precipitated product extracted with dichloromethane (500 mL). The solution was dried over sodium sulphate, filtered and concentrated. The solid residue was dried in vacuum at 40° C. yielding 1-(6-bromonaphthalen-2-yl)-ethanone (70.6 g, 99%).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09433609B2uspto-grants-2016_09