Allyl Alcohol → HCID 54461870, compound

HRID 392707Notes

Reaction equation

[C:1]1([C:7]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)([CH3:13])[C:8]([N:10]=[C:11]=[O:12])=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH2:20]([OH:23])[CH:21]=[CH2:22]>>[CH2:20]([O:23][C:11](=[O:12])[NH:10][C:8](=[O:9])[C:7]([C:1]1[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1)([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)[CH3:13])[CH:21]=[CH2:22]

Participants

Reactant 2

HCID 7858Allyl Alcohol

HCID 22661083HCID 22661083, compound

Product 1

HCID 54461870HCID 54461870, compound

Procedure

The title compound, white solid, m.p.=89° C. and MS: m/e=309.4 (M+H+) was prepared in accordance with the general method of example 1 from 2,2-diphenylpropionyl isocyanate and prop-2-en-1-ol.

Sources & evidence

ORD record: ord-bc96566ea24d4a88af94953df0d8c441
Source dataset: uspto-grants-2004_10
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US06803381B1

Reaction notes

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