Furfuryl Alcohol → HCID 22759223, compound

HRID 460861Notes

Reaction equation

[CH2:1]([OH:7])[C:2]1[O:6][CH:5]=[CH:4][CH:3]=1.[C:8]([CH:11]([CH2:23][CH2:24][CH2:25][CH:26]([OH:36])[CH2:27]OC1C=CC(F)=CC=1)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19])(=[O:10])[CH3:9]>>[C:8]([CH:11]([CH2:23][CH2:24][CH2:25][CH:26]([OH:36])[CH2:27][O:7][CH2:1][C:2]1[O:6][CH:5]=[CH:4][CH:3]=1)[CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][C:18]([O:20][CH2:21][CH3:22])=[O:19])(=[O:10])[CH3:9]

Participants

Reactant 2

HCID 7361Furfuryl Alcohol

HCID 22759236HCID 22759236, compound

Product 1

HCID 22759223HCID 22759223, compound

Procedure

The synthesis of this compound is carried out by the procedure of Example 1, Step E, except that an equivalent quantity of furfuryl alcohol is substituted for the 4-fluorophenol of Example 1, Step E.

Workup

customThe synthesis of this compound

Sources & evidence

ORD record: ord-ec9d51e582ce4391bcc3961cf3fb497f
Source dataset: uspto-grants-1977_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US04061643

Reaction notes

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