Sulfuryl chloride → Ethyl 4-chloro-3-oxo-2-[(pentyloxy)imino]butanoate

HRID 543962Notes

Reaction equation

HRID 543962 reaction equation
[CH2:1]([O:6][N:7]=[C:8]([C:14](=[O:16])[CH3:15])[C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH2:2][CH2:3][CH2:4][CH3:5].S(Cl)([Cl:20])(=O)=O>C(O)(=O)C>[CH2:1]([O:6][N:7]=[C:8]([C:14](=[O:16])[CH2:15][Cl:20])[C:9]([O:11][CH2:12][CH3:13])=[O:10])[CH2:2][CH2:3][CH2:4][CH3:5]

Participants

4

Procedure

Ethyl 2-pentyloxyimino-3-oxobutyrate (syn isomer, 57.5 g.), acetic acid (58.5 ml.) and sulfuryl chloride (20.9 ml.) were treated in a similar manner to that of Example F-(2) to give ethyl 2-pentyloxyimino-4-chloro-3-oxobutyrate (syn isomer, 51.1 g.), oil.

Sources & evidence

ORD record
ord-e87e5b2c0ba34efe8adbd04fa6cd4c1c
Source dataset
uspto-grants-1984_05
Patent number
US04447430

Reaction notes

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