HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 412931Generated: November 2, 2026
Acetyl chloride → HCID 18538454, compound
https://huagongshe.com/reaction/412931
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 18538613 | HCID 18538613 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 18538454 | HCID 18538454 | 69% |
Reaction Steps
The compound obtained in Example 13 (435 mg, 1.00 mmol). triethylamine (0.335 ml) were dissolved in THF (10 ml), and under ice cooling, to the solution was added acetyl chloride (0.142 ml). The mixture was stirred at the same temperature for 1 hour. To the reaction mixture was added a saturated aqueous solution of sodium hydrogencarbonate (15 ml) under ice cooling, and the mixture was extracted with ethyl acetate (15 ml×3). The organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The concentrate was subjected to column chromatography (silica gel log, ethyl acetate/methanol=1/0 to 9/1 to 4/1), and the desired fraction was concentrated under reduced pressure. To the concentrate was added ethyl acetate and resulting precipitates were collected by filtration. The filtrate was concentrated under reduced pressure. To the concentrate was added diethyl ether, and the resulting precipitates were collected by filtration. The precipitates were washed with diethyl ether, and dried under reduced pressure to give the titled compound (331 mg, 0.69 mmol, Yield 69%) as white crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06562978B1 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-bee9f85df1d7489ea6c3dfaf5e28bea4 |
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| Source note | uspto-grants-2003_05 |
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