HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989582Generated: October 30, 2026
Sodium Hydroxide → HCID 178448052, compound
https://huagongshe.com/reaction/989582
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 178448051 | HCID 178448051 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178448052 | HCID 178448052 | 84.8% |
Reaction Steps
Under nitrogen gas stream, a solution of 400 g (1510 mmol) of the crude 3-(trans-4-(trans-4-propylcyclohexyl)cyclohexyl)propanal obtained in the same manner as in the third step in Example 1 in 2.0 l of THF was added by drops to a mixture which was prepared by adding 43.0 g (1130 mmol) of lithium aluminum hydride to 400 ml of THF cooled down to a temperature lower than 5° C., while being maintained at the same temperature. After finishing of the adding, they were stirred at room temperature for 6 hours. This reaction mixture was gradually added to 500 ml of 2N aqueous sodium hydroxide solution and stirred at 50° C. for 30 minutes. The reaction mixture was filtered with Celite, the solvent was distilled off under a reduced pressure, and the residue was extracted with 2.0 l of ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was distilled off under a reduced pressure to obtain 341 g of a crude 3-(trans-4-(trans-4-propylcyclohexyl)cyclohexyl)propanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06458433B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-7e7a6f579a1a4ab4952ea1303cee4741 |
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| Source note | uspto-grants-2002_10 |
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