HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 126714Generated: October 27, 2026
Propargyl bromide → 4-Difluoromethyl-4-hydroxy-1-octyne
https://huagongshe.com/reaction/126714
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1,1-Difluoro-2-hexanone | HCID 21764785 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 4-Difluoromethyl-4-hydroxy-1-octyne | HCID 12786189 | — |
Reaction Steps
To a stirred suspension of 3.6 g. of magnesium and 30 mg. of mercuric chloride in 0.33 ml. of ether is added 1.5 ml. of propargyl bromide. The mixture is stirred vigorously for several minutes to initiate reaction, then a solution of 15.5 g. of 1,1-difluoro-2-hexanone and 12.1 ml. of propargyl bromide in 33 ml. of ether is added slowly (dropwise) over a 1.5 hour period, so that the mixture remains gently refluxing (25°-30° C.). After addition, the mixture is stirred at room temperature for 30 minutes, then cooled in an ice bath to 0°-5° C. and quenched by adding 35 ml. of saturated ammonium chloride solution dropwise and then stirred for 30 minutes. The mixture is filtered through Celite and washed with ether. The filtrate is concentrated in vacuo giving a yellow oil. This oil is vacuum distilled at 71° C., 12 mm giving the product as 10.54 g. of colorless oil which becomes pale yellow on standing at room temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04254036 |
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| Source dataset | uspto-grants-1981_03 |
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| ORD ID | ord-4673685a0b594870ae155c5d289032e3 |
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| Source note | uspto-grants-1981_03 |
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