5-Methylfurfural → HCID 57434516, compound

HRID 253353

Reaction equation

[I:1][CH2:2][C:3]1[N:4]=[C:5]([C:14]2C=C[C:17]([CH3:20])=[CH:16][CH:15]=2)[O:6][C:7]=1[C:8]1C=CC=CC=1.C/C(/C(C)=O)=N\[OH:24].CC1OC(C=O)=CC=1>>[I:1][CH2:2][C:3]1[N:4]=[C:5]([C:14]2[O:24][C:17]([CH3:20])=[CH:16][CH:15]=2)[O:6][C:7]=1[CH3:8]

Participants

Reactant 3

HCID 120975-Methylfurfural

HCID 64096332,3-Butanedione monoxime

HCID 574345044-Iodomethyl-5-phenyl-2-p-tolyloxazole

Product 1

HCID 57434516HCID 57434516, compound

Procedure

Analogously to the building block synthesis of 4-iodomethyl-5-phenyl-2-p-tolyloxazole, diacetylmonoxime and 5-methylfuran-2-carbaldehyde gave 4-iodomethyl-5-methyl-2-(5-methylfuran-2-yl)oxazole.

Sources & evidence

ORD record: ord-bc85954b03364772a279996244495d58
Source dataset: uspto-grants-2011_01
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07872034B2

Linked notes

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