HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1492351Generated: October 25, 2026
Methyl thiocyanate → 4-(4-n-Octylphenyl)-2-cyanophenol
https://huagongshe.com/reaction/1492351
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl thiocyanate | HCID 11168 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 4'-Octyl-[1,1'-biphenyl]-4-ol | HCID 14047211 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 4-(4-n-Octylphenyl)-2-cyanophenol | HCID 18950119 | — |
Reaction Steps
To a suspension of 2.82 g of 4-(4-n-octylphenyl) phenol in 40 ml of 1,2-dichloroethane were added under ice cooling, 6 ml of a solution of boron trichloride (2M) in 1,2-dichloroethane, and then 0.82 ml of methyl thiocyanate and 1.33 g of aluminum chloride. The mixture was stirred at room temperature until the aluminum chloride is dissolved, further stirred for 3 hours at 80° C. and cooled to room temperature. To the resulting mixture was added further 33 ml of 4N-sodium hydroxide solution. The mixture was stirred for 30 minutes at 75° to 80° C. After cooling, the reaction mixture was washed with methylene chloride. The aqueous phase was adjusted to pH2 with 6N hydrochloric acid and extracted with ether. The extract was dried and evaporated under reduced pressure to obtain crude crystals. The crystals were purified by a silica gel column chromatography to give 2.03 g of 4-(4-n-octylphenyl)-2-cyanophenol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05374373 |
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| Source dataset | uspto-grants-1994_12 |
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| ORD ID | ord-a6811cdea89441968ceecba62e61f17d |
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| Source note | uspto-grants-1994_12 |
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