Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 3-Chloropropionyl chloride | HCID 69364 | — |
| Reactant | HCID 178455850 | HCID 178455850 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 641053 | HCID 641053 | — |
Reaction Steps
3-Chloro-propionyl chloride (5.00 g) dissolved in tetrahydrofuran (50 mL) is added dropwise to a 1 M solution of allylmagnesium bromide in diethyl ether (72 mL) cooled to −15° C. The solution is warmed in the cooling bath to room temperature over a period of 2 h and stirred at room temperature overnight. Water is then added and the resulting mixture is neutralized using 4 M aqueous hydrochloric acid. The mixture is extracted with diethyl ether (3×) and the combined extracts are washed with water (2×). The organic phase is dried (Na2SO4) and the solvent is evaporated to afford the crude title compound. Yield: 7.87 g (ca. 85% pure).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08765744B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-48a1001fcdb84c3ba5712150efe30b58 |
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| Source note | uspto-grants-2014_07 |
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