3-Decynoic acid → Dec-3-enoic acid

HRID 1073651Notes

Reaction equation

HRID 1073651 reaction equation
[C:1]([OH:12])(=[O:11])[CH2:2][C:3]#[C:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]>CO.B#[Ni]>[C:1]([OH:12])(=[O:11])[CH2:2][CH:3]=[CH:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH3:10]

Participants

4

Procedure

To 4.5 g (27 mmol) of 3-decynoic acid from Example 30 dissolved in methanol in a Paar bottle is added 2 mg of nickel boride as catalyst. The bottle is flushed with hydrogen, sealed and pressurized with H2 at 2 pounds per square inch. The hydrogenation is allowed to proceed at room temperature for 2 hours. The methanol is stripped in vacuo and the residue is partitioned between ethyl acetate and in HCl. The ethyl acetate layer is separated, dried, (Na2SO4) and is stripped to afford an almost quantitative yield of 3-decenoic acid.

Workup

  1. customThe bottle is flushed with hydrogen
  2. customsealed
  3. customthe residue is partitioned between ethyl acetate and in HCl
  4. customThe ethyl acetate layer is separated
  5. customdried

Sources & evidence

ORD record
ord-35cb007cd34a4d809d2f69580f544f96
Source dataset
uspto-grants-1990_11
Patent number
US04970234

Reaction notes

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