Ethyl 2-pyridylacetate → 1-Piperidineacetic acid, ethyl ester

HRID 432811

Reaction equation

HRID 432811 reaction equation
[NH:1]1[CH2:6][CH2:5][CH2:4][CH:3](CC(OCC)=O)[CH2:2]1.[CH2:13]([O:15][C:16](=[O:24])[CH2:17]C1C=CC=CN=1)[CH3:14]>>[N:1]1([CH2:17][C:16]([O:15][CH2:13][CH3:14])=[O:24])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1

Participants

3

Reactant 2

HCID 75960Ethyl 2-pyridylacetateHCID 2760464Ethyl 2-(piperidin-3-yl)acetate

Product 1

HCID 6434661-Piperidineacetic acid, ethyl ester

Procedure

The reaction was run in the same manner as ethyl 3-piperidinylacetate, starting with commercially available ethyl-2-pyridylacetate (4.00 g; 24.5 mmol). This gave ethyl 2-piperidinylacetate (2.41 g) as a light yellow oil without further purification. MS m/z (positive ion) 172 (MH+; 100).

Workup

  1. customThis gave ethyl 2-piperidinylacetate (2.41 g) as a light yellow oil without further purification

Sources & evidence

ORD record
ord-885d55a01d27437bb29c8817847259b2
Source dataset
uspto-grants-2003_12
Patent number
US06664271B1

Linked notes

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