4-Methoxyphenol → Urethane acrylate

HRID 547873Notes

Reaction equation

HRID 547873 reaction equation
[N-:1]=[C:2]=[O:3].[C:4]([O-:17])(=[O:16])[CH2:5][CH2:6]CCCCCCCCC.C([Sn+2]CCCC)CCC.[C:27]([O-])(=[O:39])[CH2:28]CCCCCCCCCC.COC1C=CC(O)=CC=1>C1(C)C=CC=CC=1>[C:4]([OH:17])(=[O:16])[CH:5]=[CH2:6].[NH2:1][C:2]([O:39][CH2:27][CH3:28])=[O:3]

Participants

5

Conditions

Temperature
70 °C

Procedure

50 parts of toluene, 50 parts of hexamethylene diisocyanate subjected to biuret modification (“DURANATE 24A-90CX”, trade name, produced by Asahi Kasei Corporation, N.V.:), nonvolatile content: 90%, isocyanate content: 21.2%], 92 parts of polycaprolactone-modified hydroxyethyl acrylate (“PLACCEL FA2D”, trade name, produced by Daicel Chemical Industries, Ltd.), 0.02 parts of dibutyltin laurate, and 0.02 parts of hydroquinone monomethyl ether were mixed and the mixture was maintained at 70° C. for 5 hours. Thereafter, 82 parts of toluene was added to obtain a urethane acrylate having a solid content of 50% by weight. The number of repetitions of a caprolactone unit per one residue of the acrylate monomer in the obtained urethane acrylate is 2.

Sources & evidence

ORD record
ord-6773976806ed49618b6f7ed09de00b4c
Source dataset
uspto-grants-2011_05
Patent number
US07939608B2

Reaction notes

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