4-Methoxyphenol → Urethane acrylate

HRID 1892097Notes

Reaction equation

HRID 1892097 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-4c2f606e5b3c47429943da2ee952e62f
Source dataset
uspto-grants-2013_08
Patent number
US08507632B2

Reaction notes

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