HCID 68524247, compound → HCID 68526305, compound

HRID 1989851Notes

Reaction equation

HRID 1989851 reaction equation
[C:1](=[C:4]1[CH2:9][CH2:8][C:7]([CH2:11][OH:12])([CH3:10])[CH:6]=[CH:5]1)([CH3:3])[CH3:2]>C(O)(C)C>[CH:1]([C:4]1[CH2:9][CH2:8][C:7]([CH2:11][OH:12])([CH3:10])[CH2:6][CH:5]=1)([CH3:3])[CH3:2]

Participants

3

Procedure

A glass reaction vessel was charged with 1 g of 4-isopropylidene-1-methyl-2-cyclohexenylmethanol, the catalyst shown in Table 1 and 20 mL of isopropanol, and the contents of the reaction vessel were reacted with each other at a pressure of from 0.2 to 0.3 MPa and a temperature of 25° C. for the time period shown in Table 1. Thereafter, the reaction mixture was filtered to remove the catalyst therefrom, and then concentrated to obtain 4-isopropyl-1-methyl-3-cyclohexenylmethanol. The amount of hydrogen consumed and the yield of the 4-isopropyl-1-methyl-3-cyclohexenylmethanol are shown in Table 1.

Workup

  1. customA glass reaction vessel
  2. customthe contents of the reaction vessel were reacted with each other at a pressure of from 0.2 to 0.3 MPa
  3. customa temperature of 25° C.
  4. filtrationThereafter, the reaction mixture was filtered
  5. customto remove the catalyst
  6. concentrationconcentrated

Sources & evidence

ORD record
ord-a3f5c210b89744e7b6822262f1afc9ca
Source dataset
uspto-grants-2010_01
Patent number
US07642385B2

Reaction notes

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