Hydrochloric Acid → Ethyl 2-(3-chloro-4-fluoro-phenylhydrazino)propionate

HRID 544921

Reaction equation

[Cl:1][C:2]1[CH:3]=[C:4]([CH:6]=[CH:7][C:8]=1[F:9])[NH2:5].Cl.[N:11]([O-])=O.[Na+].[CH3:15][CH:16](C(C)=O)[C:17]([O:19][CH2:20][CH3:21])=[O:18].[OH-].[K+].C([O-])(=O)C.[Na+]>O.C(O)C>[Cl:1][C:2]1[CH:3]=[C:4]([NH:5][NH:11][CH:16]([CH3:15])[C:17]([O:19][CH2:20][CH3:21])=[O:18])[CH:6]=[CH:7][C:8]=1[F:9]

Participants

Conditions

Temperature: 0 °C

Procedure

A mixture of 3-chloro-4-fluoroaniline (10.0 g) in a 6 N aqueous hydrochloric acid solution (35 ml) was cooled to 0° C., and thereto was added dropwise a solution of sodium nitrite (4.80 g) in H2O (6.3 ml). After being stirred at same temperature for 25 minutes, the mixture was added to a solution of ethyl 2-methylacetoacetate (11.0 g), potassium hydroxide (21.2 g) and sodium acetate (21.2 g) in ethyl alcohol (80 ml)-H2O (100 ml) in one portion at 0° C. The resultant mixture was stirred at same temperature for 2 hours, and extracted with diethyl ether. The organic layer was washed with water twice and brine followed by being dried over sodium sulfate. The insoluble materials were filtered off, and the filtrate was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1-3:1) to give ethyl 2-(3-chloro-4-fluoro-phenylhydrazino)propionate (6.16 g) as a reddish solid. APCI-Mass m/Z 259/261 (M+H).

Workup

extractionextracted with diethyl ether
washThe organic layer was washed with water twice
dry with materialby being dried over sodium sulfate
filtrationThe insoluble materials were filtered off
customthe filtrate was evaporated under reduced pressure
customThe residue was purified by silica gel column chromatography (hexane:ethyl acetate=5:1-3:1)

Sources & evidence

ORD record: ord-0a179adff3f141c2962997c3878a5082
Source dataset: uspto-grants-2011_05
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US07935674B2

Linked notes

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