تفاعل #2286284

ord-e8a99a53e78d43f6b6903dc1f494f7c6

معادلة التفاعل

C=O
formaldehyde
C=O
formaldehyde
Cc1cccc(Cl)c1O
2-chloro-6-methyl phenol
CNC
dimethyl amine
CNC
dimethylamine
Cc1cc(CN(C)C)cc(Cl)c1O
2-chloro-4-dimethylaminomethyl-6-methyl-phenol
المردود 66.0%
Cc1cc(CN(C)C)cc(Cl)c1O
2-Chloro-4-dimethylaminomethyl-6-methyl-phenol
المردود 66.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction was heated
  2. 2
    درجة الحرارةto reflux for 24 h
  3. 3
    تركيزconcentrated under vacuum
  4. 4
    workup.ADDITIONThe resulting oil was diluted with water (200 mL)
  5. 5
    workup.ADDITIONacidified to pH=2 by addition of a 1N aqueous hydrochloric acid solution
  6. 6
    استخلاصThe water layer was extracted with ethyl acetate (300 mL)
  7. 7
    workup.ADDITIONThe water layer was made basic to pH=10 by the addition of a 1N aqueous sodium hydroxide solution
  8. 8
    استخلاصwas extracted with ethyl acetate (2×350 mL)
  9. 9
    غسيلThe organics were washed with a saturated aqueous sodium chloride solution
  10. 10
    تجفيفdried with magnesium sulfate
  11. 11
    ترشيحfiltered
  12. 12
    تركيزconcentrated under vacuum
  13. 13
    أخرىThe resulting oil was dried under high vacuum overnight

الإجراء التجريبي

A solution of 2-chloro-6-methyl phenol (5.0 g, 0.035 mol) in ethanol (25 mL) at room temperature was treated with dimethyl amine (3.95 mL of a 40% solution of dimethylamine in water, 0.035 mol) followed by formaldehyde (2.85 mL of a 37% solution of formaldehyde in water, 0.035 mol). The reaction was heated to reflux for 24 h. At this time, the reaction mixture was cooled to room temperature and concentrated under vacuum. The resulting oil was diluted with water (200 mL) and acidified to pH=2 by addition of a 1N aqueous hydrochloric acid solution. The water layer was extracted with ethyl acetate (300 mL). The ethyl acetate layer was discarded. The water layer was made basic to pH=10 by the addition of a 1N aqueous sodium hydroxide solution and was extracted with ethyl acetate (2×350 mL). The organics were washed with a saturated aqueous sodium chloride solution, dried with magnesium sulfate, filtered and concentrated under vacuum. The resulting oil was dried under high vacuum overnight to afford 2-chloro-4-dimethylaminomethyl-6-methyl-phenol (2b) (4.62 g, 66%) as an off-white solid; EI(+)-HRMS m/z calcd for C10H14ClNO (M+) 199.0764, found 199.0767. Molecular Weight=199.6822; Exact Mass=199.0764

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: USRE046024E1uspto-grants-2016_06