Phenol → phenyl N-methacryloylcarbamate

HRID 2107538Notes

Reaction equation

HRID 2107538 reaction equation
[C:1]([N:6]=[C:7]=[O:8])(=[O:5])[C:2]([CH3:4])=[CH2:3].[C:9]1([OH:15])[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1>ClCCCl.C(Cl)(Cl)Cl>[C:1]([NH:6][C:7](=[O:8])[O:15][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)(=[O:5])[C:2]([CH3:4])=[CH2:3]

Participants

5

Reactant 2

HCID 996PhenolHCID 10942374Methacryloyl isocyanate

Product 1

HCID 14817887phenyl N-methacryloylcarbamate

Reagents, catalysts & solvents 2

HCID 111,2-DichloroethaneSolvent2×HCID 6212ChloroformSolvent2×

Procedure

A solution of methacryloyl isocyanate (11.1 g; 0.1 mol) in 1,2-dichloroethane (50 ml) was dropise added to a solution of dry phenol (9.4 g; 0.1 mol) in chloroform (20 ml) under nitrogen stream while cooling with ice. After completion of the addition, chloroform and 1,2-dichloroethane were evaporated under reduced pressure. The residue (20.5 g) was recrystallized from a mixture of hexane and benzene to give phenyl N-methacryloylcarbamate as colorless needles. M.P., 94°-95° C.

Workup

  1. temperaturewhile cooling with ice
  2. customwere evaporated under reduced pressure
  3. customThe residue (20.5 g) was recrystallized from a mixture of hexane and benzene

Sources & evidence

ORD record
ord-8644a3efeee0480a900a02b92d506841
Source dataset
uspto-grants-1990_06
Patent number
US04935413

Reaction notes

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