HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1380780Generated: October 31, 2026
Aluminium lithium hydride → HCID 178444272, compound
https://huagongshe.com/reaction/1380780
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 178444271 | HCID 178444271 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178444272 | HCID 178444272 | 96% |
Reaction Steps
A mixture of 930 mg of lithium aluminium hydride in 100 ml of absolute tetrahydrofuran was placed at 0° C. in a sulphonation flask and treated within 20 minutes with a solution of 8.2 g of 4'-(trans-4-pentylcyclohexyl)-4-biphenylcarboxaldehyde in 100 ml of absolute tetrahydrofuran. After completion of the addition, the mixture was stirred for a further 2 hours while warming to room temperature, subsequently cautiously quenched with 100 ml of 1N sulphuric acid and extracted three times with 200 ml of methylene chloride each time. The organic phases were washed twice with 100 ml of water each time, dried over magnesium sulphate and concentrated. There were obtained 7.90 g (96%) of 4'-(trans-4-pentylcyclohexyl)-4-biphenylmethanol as a colourless, crystalline mass (purity 99.4% in accordance with gas chromatography) which was used in the following step without further purification. M.p. 180.4° C.; Rf value [petroleum ether/ethyl acetate (9:1)]: educt 0.70, product 0.30.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04583826 |
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| Source dataset | uspto-grants-1986_04 |
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| ORD ID | ord-0a444a6b48bd447caf4823eaf924fe0d |
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| Source note | uspto-grants-1986_04 |
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