반응 #806259

ord-b93164d19668495195d8b6e481c150c9

반응 방정식

CC(C)C(O)C(C)(C)CO
2,2,4-trimethylpentan-1,3-diol
[Na+].[OH-]
NaOH
C=C(C)CCl
methallyl chloride
C=C(C)COCC(C)(C)C(O)C(C)C
1-(2-methyl-2-propenyloxy)-2,2,4-trimethylpentan-3-ol
수율 101.8%

반응 조건

온도
100°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타To a 1 L flask equipped with a reflux condenser
  2. 2
    온도This mixture was heated in an oil bath
  3. 3
    기타reached 50° C.
  4. 4
    workup.ADDITIONDuring the addition
  5. 5
    온도The reaction mixture was cooled
  6. 6
    기타quenched with 400 ml of water
  7. 7
    추출extracted twice with 100 ml of toluene
  8. 8
    세척The combined organic layers were washed with 50 ml of saturated ammonium chloride and 50 ml of saturated sodium chloride
  9. 9
    기타evaporated

실험 절차

To a 1 L flask equipped with a reflux condenser and a thermometer, was added 292.5 g (2.0 mol) of 2,2,4-trimethylpentan-1,3-diol, 352.0 g (4.4 mol) of 50% aqueous NaOH, and 6.45 g (20 mmol) of tetrabutyl ammonium bromide. This mixture was heated in an oil bath and when the reaction mixture reached 50° C., 199.2 g (2.2 mol) of methallyl chloride was added drop-wise over 50 minutes. During the addition, the oil bath temperature was gradually raised to 100° C. and the reaction was continued for an additional 3 hours at 100° C. The reaction mixture was cooled, quenched with 400 ml of water, and extracted twice with 100 ml of toluene. The combined organic layers were washed with 50 ml of saturated ammonium chloride and 50 ml of saturated sodium chloride and evaporated to give 408 g of crude 1-(2-methyl-2-propenyloxy)-2,2,4-trimethylpentan-3-ol. After reduced pressure distillation (71–80° C., 3 mmHg), 377.1 g (yield 94.1%) of 1-(2-methyl-2-propenyloxy)-2,2,4-trimethylpentan-3-ol was obtained.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07132391B2uspto-grants-2006_11