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65695-05-8

65695-05-8 Structure

65695-05-8 Structure
IdentificationBack Directory
[Name]

METHYL 4-[(Z)-AMINO(HYDROXYIMINO)METHYL]BENZOATE
[CAS]

65695-05-8
[Synonyms]

Methyl 4-(N-hydroxycarbamimidoyl)
Methyl 4-(N-hydroxycarbaMiMidoyl)benzoate
Methyl 4-[amino(hydroxyimino)methyl]benzoate
(E)-Methyl 4-(N'-hydroxycarbaMiMidoyl)benzoate
methyl 4-[(Z)-N'-hydroxycarbamimidoyl]benzoate
METHYL 4-[(Z)-AMINO(HYDROXYIMINO)METHYL]BENZOATE
METHYL 4-[AMINO(HYDROXYIMINO)METHYL]BENZENECARBOXYLATE
4-[(HYDROXYAMINO)IMINOMETHYL]-BENZOIC ACID, METHYL ESTER
Benzoic acid,4-[(hydroxyaMino)iMinoMethyl]-, Methyl ester
Benzoic acid, 4-[(hydroxyamino)iminomethyl]-, methyl ester (9CI)
[Molecular Formula]

C9H10N2O3
[MDL Number]

MFCD08689689
[MOL File]

65695-05-8.mol
[Molecular Weight]

194.19
Chemical PropertiesBack Directory
[Melting point ]

172-174
[Boiling point ]

327.2±44.0 °C(Predicted)
[density ]

1.28±0.1 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[form ]

solid
[pka]

13.88±0.50(Predicted)
[color ]

White
Safety DataBack Directory
[Hazard Codes ]

Xi,T
[Risk Statements ]

25
[Safety Statements ]

45
[HazardClass ]

IRRITANT
[HS Code ]

2921490090
Hazard InformationBack Directory
[Synthesis]

Methyl 4-cyanobenzoate

1129-35-7

METHYL 4-[(Z)-AMINO(HYDROXYIMINO)METHYL]BENZOATE

65695-05-8

General procedure for the synthesis of methyl 4-(N-hydroxyformamidinyl)benzoate (IV) from methyl 4-cyanobenzoate (III): methyl 4-cyanobenzoate (III) (2.50kg, 1wt) was dissolved in methanol (7.5L, 3vol) and diluted with methyl tert-butyl ether (9.3kg, 3.7wt). Aqueous hydroxylamine (50% solution; 1.23 kg, 0.5 wt, 1.2 eq.) was added slowly over about 0.5 h at 20-25 °C. The dosing line was flushed with methanol (1 kg, 0.4 wt) and the reaction was kept at 20-25 °C for about 12 hours. Upon completion of the reaction, the reaction mixture was cooled to 5±5°C and aged at this temperature for 3 hours. The product, methyl 4-(N'-hydroxyformamidinyl)benzoate (IV), was isolated by filtration, washed with methyl tert-butyl ether (2 x 5.5 kg, 2 x 2.2 wt) and dried under a stream of nitrogen for about 4 h to give the product (2.38 kg, 93% yield).

[References]

[1] Patent: WO2017/220446, 2017, A1. Location in patent: Page/Page column 26
[2] Journal of Labelled Compounds and Radiopharmaceuticals, 2012, vol. 55, # 2, p. 71 - 79
[3] Organic Letters, 2017, vol. 19, # 11, p. 2885 - 2888
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