تفاعل #955449

ord-d073c40e71284b40b5f9822718a6bab9

معادلة التفاعل

O=N[O-].[Na+]
sodium nitrite
Cc1c(F)ccc(N)c1Cl
2-chloro-4-fluoro-3-methylaniline
Cl
hydrochloric acid
F[B-](F)(F)F.[Na+]
sodium tetrafluroborate
Cc1c(F)ccc([N+]#N)c1Cl.F[B-](F)(F)F
2-chloro-4-fluoro-3-methylbenzenediazonium tetrafluoroborate
المردود 83.6%

المذيبات

ظروف التفاعل

درجة الحرارة
5°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    ترشيحThe resultant yellow solution after filtration
  2. 2
    درجة الحرارةwas cooled to 0° C. and with stirring sodium tetrafluoroborate (71 g) in water (140 ml)
  3. 3
    workup.ADDITIONadded dropwise
  4. 4
    أخرىThe yellow solid formed
  5. 5
    ترشيحwas filtered off
  6. 6
    غسيلwashed with petroleum ether (6.p 60°-80°)
  7. 7
    أخرىobtained
  8. 8
    workup.ADDITIONby treating the filtrate
  9. 9
    تجفيفThe solid was dried overnight over phosphorus pentoxide in vacuo

الإجراء التجريبي

2-chloro-4-fluoro-3-methylaniline (73 g) was added dropwise, with vigorous stirring to 50% hydrochloric acid (256 ml). The resulting white suspension was cooled to 5° C. and with stirring, sodium nitrite (34.5 g) in water (50 ml), added dropwise. The resultant yellow solution after filtration was cooled to 0° C. and with stirring sodium tetrafluoroborate (71 g) in water (140 ml), added dropwise. The yellow solid formed was filtered off and washed with petroleum ether (6.p 60°-80°) and combined with further similarly washed solid obtained by treating the filtrate, maintained at 0° C., with sodium tetrafluroborate (71 g) in water (140 ml). The solid was dried overnight over phosphorus pentoxide in vacuo, giving a yield of 98.8 g 2-chloro-4-fluoro-3-methylbenzenediazonium tetrafluoroborate. This was divided into three protions each being placed in a round-bottomed flask (250 ml). The flasks were in turn heated with a naked bunsen flame until decomposition set in and an orange vapor was emitted, which was condensed and collected in a cooled receiver. The orange oil obtained from the three batches was dissolved in diethyl ether (200 ml) and washed with aqueous sodium hydroxide solution (10%, 300 ml) then saturated brine (200 ml). After drying the ethereal solution over anhydrous magnesium sulphate, filtering and evaporating at atmospheric pressure, the residual oil was distilled to give 2-chloro-3,6-difluorotoluene (45 g)

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US04778822uspto-grants-1988_10