HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1246584Generated: October 31, 2026
Propionyl chloride → HCID 15156825, compound
https://huagongshe.com/reaction/1246584
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Propionyl chloride | HCID 62324 | — |
| Reactant | 1-Phenylethenyl acetate | HCID 75153 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15156825 | HCID 15156825 | 14% |
Reaction Steps
A solution of 8.11 g (50 mmol) of 1-phenylvinyl acetate (prepared as described in Example 1) in 80 ml of anhydrous tetrahydrofuran was placed in a 500 ml round bottomed flask and cooled to −75°. A solution of 6.16 g (55 mmol) of potassium tert-butylate in 60 ml of anhydrous tetrahydrofuran was slowly added (40′) and the mixture was stirred for 1 h at −75°. A solution of propionyl chloride (55 mmol) in 20 ml of anhydrous tetrahydrofuran was slowly added (20′) and, after 2 h at −75°, the cooling bath was removed and 60 ml of a saturated solution of NaHCO3 was rapidly added. The temperature rose rapidly to −10° and the mixture was extracted with ether. After usual workup, the product was purified by flash chromatography (SiO2, pentane/ether 8/2), bulb-to-bulb distillation and preparative GC using a 1.2 m×6 mm column loaded with 10% SE-30 on Supelcoport® 80–100 mesh, vector gas: helium at 30 ml/min. The product was obtained in 14% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07129206B2 |
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| Source dataset | uspto-grants-2006_10 |
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| ORD ID | ord-14a127be1d174f1fa5f3c3d99b22c6d9 |
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| Source note | uspto-grants-2006_10 |
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