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865106-51-0

4-(CYCLOPROPYLMETHOXY)PIPERIDINE synthesis

2synthesis methods
-

Yield:865106-51-0 100%

Reaction Conditions:

with trifluoroacetic acid in dichloromethane at 20;

Steps:

27.2 The second step: 4-cyclopropylmethoxypiperidine (27B)

Dissolve 4-cyclopropylmethoxypiperidine-1-carboxylic acid tert-butyl ester 27A (870mg, 3.41mmol) in 20mL of dichloromethane, add 5mL of trifluoroacetic acid, and react overnight at room temperature.LC-MS monitoring showed that the reaction was complete. The reaction liquid is adjusted to alkaline with sodium carbonate aqueous solution,It was extracted 3 times with 20 mL of dichloromethane, the dichloromethane layers were combined, dried, and spin-dried to give the product 4-cyclopropylmethoxypiperidine 27B (530 mg, 100%) as a yellow oil.

References:

CN111848591,2020,A Location in patent:Paragraph 0520-0521; 0524-0525