Ammonium formate → HCID 85362584, compound

HRID 618574Notes

Reaction equation

[CH3:1][C:2]([CH:13]=[CH:14][C:15]1[C:20]([CH3:22])([CH3:21])[CH2:19][CH2:18][C:17](=[O:23])[C:16]=1[CH3:24])=[C:3]=[CH:4][P:5](=[O:12])([O:9][CH2:10][CH3:11])[O:6][CH2:7][CH3:8].C([O-])=O.[NH4+]>>[CH3:1][C:2]([CH:13]=[CH:14][C:15]1[C:20]([CH3:22])([CH3:21])[CH2:19][CH2:18][C:17](=[O:23])[C:16]=1[CH3:24])=[CH:3][CH2:4][P:5](=[O:12])([O:6][CH2:7][CH3:8])[O:9][CH2:10][CH3:11]

Participants

Reactant 2

HCID 2723923Ammonium formate

HCID 85398784HCID 85398784, compound

Product 1

HCID 85362584HCID 85362584, compound

Procedure

reacting the 3-methyl-5-(2,6,6-trimethyl-3-oxocyclohex-1-enyl)-1,2,4-pentatrienylphosphonic acid, diethyl ester with ammonium formate or a trialkylammonium formate to form 3-methyl-5-(2,6,6-trimethyl-3-oxocyclohex-1-enyl)-2,4-pentadienylphosphonic acid, diethyl ester; and

Sources & evidence

ORD record: ord-0118c37caf6745b3b35589d6f84abade
Source dataset: uspto-grants-1999_09
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05952519

Reaction notes

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