反応 #312597

ord-b70a2714260e4d0b9b4126216df3bcbd

反応方程式

ClCC1CO1
Epichlorohydrin
CC(C)(C)[O-].[K+]
potassium tert-butoxide
ClCC1CO1
epichlorohydrin
CCCCCC(CO)CCC
2-propylheptanol
CCCCCC(CCC)COCC(O)CCl
1-chloro-3-(2-propyl-heptyloxy)-propan-2-ol
CCCCCC(CCC)COCC(O)CCl
1-chloro-3-(2-propyl-heptyloxy)-propan-2-ol
CCCCCC(CCC)COCC1CO1
2-propylheptyl glycidyl ether

反応条件

温度
90°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他To a flame dried
  2. 2
    その他500 mL round bottomed flask equipped with an addition funnel
  3. 3
    workup.DISTILLATIONis distilled at a temperature range of 90° C.→95° C. under 0.2 mm Hg
  4. 4
    workup.STIRRINGstirred at RT under an argon atmosphere
  5. 5
    workup.STIRRINGthe suspension is stirred at RT for 18 hours
  6. 6
    その他The reaction is then evaporated to dryness, residue
  7. 7
    workup.DISSOLUTIONdissolved in hexanes
  8. 8
    洗浄washed with water (100 mL)
  9. 9
    その他The hexanes phase is separated
  10. 10
    乾燥dried with Na2SO4
  11. 11
    ろ過filtered
  12. 12
    その他evaporated to dryness

実験手順

To a flame dried, 500 mL round bottomed flask equipped with an addition funnel charged with epichlorohydrin (15.62 gm., 0.17 moles), is added 2-propylheptanol (Pfaltz & Bauer, Inc., 172 E. Aurora Street, Waterbury Conn., 06708, USA) (20 gm., 0.127 moles) and stannic chloride (0.20 gm., 0.001 moles). The reaction is kept under an argon atmosphere and warmed to 90° C. using an oil bath. Epichlorohydrin is dripped into the stirring solution over 60 minutes followed by stirring at 90° C. for 18 hours. The reaction is fitted with a vacuum distillation head and 1-chloro-3-(2-propyl-heptyloxy)-propan-2-ol is distilled at a temperature range of 90° C.→95° C. under 0.2 mm Hg. Wt.=22.1 gm. The 1-chloro-3-(2-propyl-heptyloxy)-propan-2-ol (5.0 gm., 0.020 moles) is dissolved in tetrahydrofuran (50 mL) and stirred at RT under an argon atmosphere. To the stirring solution is added potassium tert-butoxide (2.52 gm., 0.022 moles) and the suspension is stirred at RT for 18 hours. The reaction is then evaporated to dryness, residue dissolved in hexanes and washed with water (100 mL). The hexanes phase is separated, dried with Na2SO4, filtered and evaporated to dryness to yield the crude 2-propylheptyl glycidyl ether, which can be further purified by vacuum distillation.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US07557076B2uspto-grants-2009_07