HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 992450Generated: November 1, 2026
Propargyl bromide → HCID 18412031, compound
https://huagongshe.com/reaction/992450
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propargyl bromide | HCID 7842 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | HCID 10775653 | HCID 10775653 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18412031 | HCID 18412031 | — |
Reaction Steps
3.3 ml of butyl lithium (1.6 molar in hexane) are added under stirring to a solution of 0.8 ml diisopropylamine in 20 ml tetrahydrofurane at −78° C. under nitrogen. After stirring for 30 minutes at the same temperature, 1.13 g of 5-(4-chloro-phenyl )-2,2-dimethyl-(1,3)-dioxolan-4-one in 5 ml tetrahydrofurane are added and stirring is continued for 1.5 hours. Then the reaction mixture is treated with a solution of 0.57 ml propargyl bromide in 3 ml tetrahydrofurane. Stirring is continued at about 60° C. over the night. Then the reaction is quenched with HCl 1N (pH 6) and ice and water and extracted with diethyl ether. The extracts are dried over sodium sulfate and evaporated. The 5-(4-chloro-phenyl)-2,2-dimethyl-5-prop-2-ynyl-(1,3)dioxolan-4-one remains as a oil which is used directly for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06469005B1 |
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| Source dataset | uspto-grants-2002_10 |
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| ORD ID | ord-3b0a3608dc1748cf8df2beba08d96d1d |
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| Source note | uspto-grants-2002_10 |
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