Stearyl Alcohol → Heptadecane

HRID 339310

Reaction equation

HRID 339310 reaction equation
[CH2:1](O)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17]C.[H][H]>[Ni]>[CH3:17][CH2:16][CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][CH2:9][CH2:8][CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2][CH3:1]

Participants

4

Reactant 2

HCID 8221Stearyl AlcoholHCID 178418361HCID 178418361, compound

Product 1

HCID 12398Heptadecane

Reagents, catalysts & solvents 1

HCID 935NickelCatalyst

Conditions

Temperature
240 °C

Procedure

1000 g of 1-octadecanol (Lorol C18 from Cognis) were initially charged in a stirrable pressure vessel with 10 g of a nickel catalyst (Ni-5249 P from Engelhard; Ni content=63% by weight) and heated to 240° C. Subsequently, over a period of 12 h, hydrogen was added through a sparging tube at a pressure of 20 bar and the reaction gases were simultaneously discharged through a valve in the reactor lid. Thereafter, the product was cooled, discharged and filtered. This reaction product was fractionated in a distillation to give pure heptadecane and then deodorized with nitrogen. This gives a colorless, low-odor product which is liquid at 40° C.

Workup

  1. customthe reaction gases
  2. customwere simultaneously discharged through a valve in the reactor lid
  3. temperatureThereafter, the product was cooled
  4. filtrationfiltered
  5. distillationThis reaction product was fractionated in a distillation

Sources & evidence

ORD record
ord-46cbc7c7cc4a471bb26f0238a7604d4b
Source dataset
uspto-grants-2014_11
Patent number
US08895039B2

Linked notes

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