반응 #335743

ord-1e8c1da2e5614c19ab8e3fcde4afadf9

반응 방정식

C=CCCCCBr
6-bromo-1-hexene
N[C@H]1[C@H]([C@H](O)[C@H](O)CO)OC(O)(C(=O)O)C[C@@H]1O
Neu
Clc1ccc(Cl)cc1
1,4-dichlorobenzene
[Mg]
magnesium
Cl
hydrochloric acid
C=CCCCCc1ccc(Cl)cc1
4-(5-hexenyl)-1-chlorobenzene
수율 40.0%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The mixture was subsequently heated at 80° to 84° C. for an additional 2 hours
  2. 2
    기타decanted off from the excess magnesium
  3. 3
    workup.ADDITIONThe resultant solution of Grignard compound was added dropwise at 80° C. over a period of 30 minutes to a stirred solution
  4. 4
    workup.ADDITIONpoured onto ice
  5. 5
    추출extracted three times
  6. 6
    workup.ADDITIONa 1:1 mixture of diethyl ether/methyl tert-butyl ether
  7. 7
    workup.STIRRINGthe ether fractions were stirred with activated charcoal
  8. 8
    건조dried over sodium sulfate
  9. 9
    기타After the filtrate had been evaporated

실험 절차

A solution containing 294 g (2 Mol) of 1,4-dichlorobenzene in 500 ml of anhydrous tetrahydrofuran was added dropwise at 80° C. under nitrogen over a period of 110 minutes to a stirred suspension of 48.6 g (2.0 Mol) of magnesium turnings. The mixture was subsequently heated at 80° to 84° C. for an additional 2 hours, then decanted off from the excess magnesium. The resultant solution of Grignard compound was added dropwise at 80° C. over a period of 30 minutes to a stirred solution containing 194 g (1.8 Mol) of 6-bromo-1-hexene (commercially available from Fluka GmbH, D-7910 Neu-Ulm) in 200 ml of tetrahydrofuran. The mixture was then stirred at 80° for an additional four hours and poured onto ice. The mixture was acidified using hydrochloric acid and extracted three times using a 1:1 mixture of diethyl ether/methyl tert-butyl ether, and the ether fractions were stirred with activated charcoal and dried over sodium sulfate. After the filtrate had been evaporated, the residue was fractionated under reduced pressure. About 156 g (corresponding to a yield of 40 percent of theory) of 4-(5-hexenyl)-1-chlorobenzene were obtained at a pressure of 13 hPa and at a temperature of 116° to 118° C. 4-(4-pentenyl)-1-chlorobenzene (b.p. 102° to 105° C. at 13 hPa), 4-(11-dodecenyl)-1-chlorobenzene (b.p. 147° to 150° at 0.2 hPa) and 4-(8-nonenyl)-1-chlorobenzene (b.p. 87° C. at 0.3 hPa) can also be prepared in the same manner.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05210247uspto-grants-1993_05