تفاعل #667977

ord-77fbf36e757c4803bb95a2bcc5bd85e6

معادلة التفاعل

C=CC(=O)OCCCCOC(=O)OCCl
Chloromethyl 4-acryloyloxybutyl carbonate
C=CC(=O)[O-].[K+]
potassium acrylate
C=CC(=O)OCCCCOC(=O)OCOC(=O)C=C
title product
المردود 91.1%
C=CC(=O)OCCCCOC(=O)OCOC(=O)C=C
Acryloyloxymethyl 4-acryloyloxybutyl carbonate
المردود 91.1%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىAfter 5 days at 20° C. the solvent is removed under reduced pressure
  2. 2
    workup.DISSOLUTIONthe residue dissolved
  3. 3
    workup.ADDITIONby adding dichloromethane (60 ml) and water (30 ml)
  4. 4
    أخرىAfter separating the phases the aqueous layer
  5. 5
    استخلاصis extracted with dichloromethane (3×30 ml)
  6. 6
    غسيلthe combined organic phase washed with saturated aqueous sodium hydrogen carbonate (50 ml)
  7. 7
    تجفيفThe organic phase is dried (MgSO4)
  8. 8
    أخرىthe solvent removed under reduced pressure

الإجراء التجريبي

Chloromethyl 4-acryloyloxybutyl carbonate (1.183 g, 5.00 mmol) prepared as described in Example 8 is added to a suspension of freeze dried potassium acrylate (0.606 g, 5.50 mmol) and 18-crown-6 (0.066 g, 0.25 mmol) in dimethylformamide (50 ml) under a dry N2 atmosphere. After 5 days at 20° C. the solvent is removed under reduced pressure and the residue dissolved by adding dichloromethane (60 ml) and water (30 ml). After separating the phases the aqueous layer is extracted with dichloromethane (3×30 ml) and the combined organic phase washed with saturated aqueous sodium hydrogen carbonate (50 ml). The organic phase is dried (MgSO4) and the solvent removed under reduced pressure to give 1.24 g (91%) of the title product. 1H NMR (60 MHz, CDCl3): δ 1.82 (4H, m, CH2 --CH2), 4.23 (4H, m, 2×CH2 --O), 5.88 (2H, s, O--CH2 --O), 5.7-6.8 (6H, 2×CH=CH2).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05919753uspto-grants-1999_07