ChemicalBook--->CAS DataBase List--->77925-80-5

77925-80-5

77925-80-5 Structure

77925-80-5 Structure
IdentificationBack Directory
[Name]

N-(Benzyloxy)-2-nitrobenzenesulfonaMide
[CAS]

77925-80-5
[Synonyms]

N-(Benzyloxy)-2-nitrobenzenesulfonaMide
N-(benzyloxy)-2-nitrobenzene-1-sulfonamide
Benzenesulfonamide, 2-nitro-N-(phenylmethoxy)-
[Molecular Formula]

C13H12N2O5S
[MDL Number]

MFCD23135238
[MOL File]

77925-80-5.mol
[Molecular Weight]

308.31
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
Hazard InformationBack Directory
[Synthesis]

O-Benzylhydroxylamine hydrochloride

2687-43-6

2-Nitrobenzenesulfonyl chloride

1694-92-4

N-(Benzyloxy)-2-nitrobenzenesulfonaMide

77925-80-5

A solution of 2-nitrobenzene-1-sulfonyl chloride (500 g, 2.26 mol) in pyridine (1500 mL) was slowly added dropwise to a solution of O-benzylhydroxylamine hydrochloride (400 g, 2.51 mol) in pyridine (1500 mL) at 0 °C. The reaction mixture was then stirred at 20 °C overnight. After completion of the reaction, the mixture was concentrated under reduced pressure, diluted with dichloromethane (DCM) and washed three times with 10% hydrochloric acid solution. After combining the organic layers, the mixture was again concentrated under reduced pressure and recrystallized by dichloromethane to give N-(benzyloxy)-2-nitrobenzenesulfonamide as a yellow solid (485 g, 62.6% yield).

[References]

[1] Chemistry - A European Journal, 2018, vol. 24, # 32, p. 8081 - 8086
[2] Synthesis, 2001, # 7, p. 1086 - 1092
[3] Journal of Organic Chemistry, 2015, vol. 80, # 12, p. 6076 - 6082
[4] Patent: US2013/289012, 2013, A1. Location in patent: Paragraph 0199; 0200
[5] Patent: US2013/296555, 2013, A1. Location in patent: Paragraph 0231; 0232
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