Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Aluminum | HCID 5359268 | — |
| Reactant | HCID 13259981 | HCID 13259981 | — |
| Catalyst | Mercuric Chloride | HCID 24085 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13259985 | HCID 13259985 | 74.8% |
Reaction Steps
1.58 g (0.058 mol) of aluminum (in the form of flakes) are covered with a layer of 7.3 ml of tetrahydrofuran, and a catalytic amount (0.05 g) of mercury(II) chloride and an iodine crystal are added. After the mixture has stood for 12 hours at 20° C., 10.3 g (0.087 mol) of propargyl bromide in 11 ml of tetrahydrofuran are added dropwise at 60° C. The mixture is then cooled to -60° C., and a solution of 17.1 g (0.05 mol) of 5-(2,4-dichlorophenoxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)pentan-2-one in 20 ml of tetrahydrofuran is added dropwise. The mixture is allowed to warm up to 0° C. and is kept for a further hour at this temperature, and 22 ml of a saturated, aqueous ammonium chloride solution are added. Thereafter, the mixture is filtered, the filtrate is evaporated down in vacuo and the residue is taken up in 200 ml of ethyl acetate. After the solution has been washed with three times 100 ml of water, the organic phase is dried over sodium sulphate and then evaporated down in vacuo. Residues of solvent are removed at 50° C. and 0.01 mbar. 14.3 g (74.8% of theory) of 7-(2,4-dichlorophenoxy)-5,5-dimethyl-4-(1,2,4-triazol-1-yl-methyl)-hept-1-in-4-ol are obtained as a brownish oil of refractive index nD20 =1.5642.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04578396 |
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| Source dataset | uspto-grants-1986_03 |
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| ORD ID | ord-8581513d304c4e70beb2dd859e76000d |
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| Source note | uspto-grants-1986_03 |
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