tert-Butyl acrylate → Hydroxystyrene

HRID 840047

Reaction equation

HRID 840047 reaction equation
C([O:4][CH:5]=[CH:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1)(=O)C.C(OC(C)(C)C)(=O)C=C>C1(C)C=CC=CC=1>[OH:4][CH:5]=[CH:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1

Participants

4

Conditions

Temperature
60 °C

Procedure

A 22 L reactor was charged with 2.919 kg acetoxystyrene, 1.538 kg t-butyl acrylate, 231 g BPO and 6 L toluene. The reactor was purged with nitrogen, and the reaction solution was heated at 60° C. under a N2 atmosphere for 23 h. The solution was then cooled to room temperature, diluted with an additional 12 L of toluene, and 248 L of heptane:isopropyl alcohol (30:1) was added. The precipitate was collected by vacuum filtration, and washed with 24 L heptane. The solid was recrystalized by first dissolving it in 15 L acetone and then adding 300 L isopropyl alcohol:water (51:24 v/v). The product was collected by vacuum filtration, rinsed with 30 L 1:1 isoproyl alcohol:water, and then dried at 50-55° C. under vacuum to a constant weight.

Workup

  1. customThe reactor was purged with nitrogen
  2. temperatureThe solution was then cooled to room temperature
  3. additiondiluted with an additional 12 L of toluene, and 248 L of heptane:isopropyl alcohol (30:1)
  4. additionwas added
  5. filtrationThe precipitate was collected by vacuum filtration
  6. washwashed with 24 L heptane
  7. customThe solid was recrystalized
  8. dissolutionby first dissolving it in 15 L acetone
  9. additionadding 300 L isopropyl alcohol:water (51:24 v/v)
  10. filtrationThe product was collected by vacuum filtration
  11. washrinsed with 30 L 1:1 isoproyl alcohol
  12. dry with materialwater, and then dried at 50-55° C. under vacuum to a constant weight

Sources & evidence

ORD record
ord-4990dfe89939464a9a677cbd8c4759f1
Source dataset
uspto-grants-2002_04
Patent number
US06365321B1

Linked notes

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