تفاعل #725862
ord-0a061b946840442b92f8a92186f182c9
معادلة التفاعل
4-fluoroaniline
HCl
dimethyl dihydroxyfumarate
→
2,3-bis-(4-fluoroanilino)-but-2-enedioic acid dimethyl ester
المردود 63.0%
الكواشف
لا شيء
المذيبات
ظروف التفاعل
الظروف التفصيلية
See reaction.notes.procedure_details.
المعالجة
- 1درجة الحرارةheated
- 2درجة الحرارةto reflux for 3 hours
- 3ترشيحThe next morning, the resulting thick paste was filtered on a coarse frit
- 4غسيلwashed with a 50% (v:v) methanol-water mixture
- 5أخرىdried in a vacuum oven
- 6أخرىyielding 32.4 g (63% yield) which
- 7workup.ADDITIONa mixture of E/Z isomers (E:Z˜1:2)
الإجراء التجريبي
In a round bottom flask with a teflon stirbar, 25 g (142 mmol) of dimethyl dihydroxyfumarate (prepared according to a procedure described in U.S. Pat. No. 3,334,102), 34.7 g (312.5 mmol) of 4-fluoroaniline, 0.1 mL of concentrated HCl, and 90 ml of methyl alcohol were mixed and heated to reflux for 3 hours. The reaction mixture was cooled to room temperature and left overnight in a refrigerator. The next morning, the resulting thick paste was filtered on a coarse frit, washed with a 50% (v:v) methanol-water mixture, and dried in a vacuum oven, yielding 32.4 g (63% yield) which, according to NMR analysis, was a mixture of E/Z isomers (E:Z˜1:2).