N-pentylidenehydroxylamine

Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

Procedure: As described for example 1a except using valeraldehyde (12.4 mL, 116 mmol) instead of butyraldehyde, the penatnal oxime intermediate product (11.7 g, 99%) was obtained as a yellow solid and as a mixture of cis and trans isomers that was used directly without further purification. MS (EI): m/e=101.0 [M]+. Then as described for example 1b, except using (E and/or Z)-pentanal oxime (11.4 g, 113 mmol) instead of (E and/or Z)-butanal oxime, and using ethyl 3,3-dimethylaminoacrylate instead of ethyl (E)-3-(1-pyrrolidino)-2-butenoate, the title compound (13.6 g, 61%) was obtained as a yellow liquid after purification by chromatography (silica, 0 to 10% ethyl acetate in heptane). MS: m/e=198.1 [M+H]+. was used directly without further purification