HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343637Generated: October 31, 2026
3-Chloro-1-propanol → HCID 13796792, compound
https://huagongshe.com/reaction/343637
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chloro-1-propanol | HCID 12313 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 4'-Hydroxy-4-biphenylcarbonitrile | HCID 140610 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13796792 | HCID 13796792 | 21% |
Reaction Steps
Into a 300 ml flask, 20 g (102.4 mmol) of 4-cyano-4'-hydroxybiphenyl, 140 ml of ethanol and a NaOH aqueous solution (7.48 g (132.2 mmol) of NaOH/40 ml of water) were added. The mixture was stirred at 80° C. for 10 minutes, and then 10.66 g (112.8 mmol) of 3-chloro-1-propanol was added thereto. The mixture was heated and refluxed for 18 hours. Ethanol was distilled off. Then, 300 ml of water was added to the reaction solution, and the mixture was neutralized with hydrochloric acid. Precipitated crystals were collected by filtration. Then, 1200 ml of toluene was added thereto, and the toluene layer was washed with water and a saturated sodium chloride aqueous solution and then dried over anhydrous sodium sulfate. Further, the solvent was distilled off under reduced pressure, and the residue was recrystallized from ethanol to obtain 5.34 g (yield: 21%) of 4-cyano-4'-(3-hydroxypropoxy)biphenyl (7) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05861534 |
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| Source dataset | uspto-grants-1999_01 |
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| ORD ID | ord-7361219e85414bcaba7426a76ec0203c |
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| Source note | uspto-grants-1999_01 |
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