HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 565628Generated: October 30, 2026
Acetyl chloride → HCID 22110983, compound
https://huagongshe.com/reaction/565628
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | HCID 22111064 | HCID 22111064 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22110983 | HCID 22110983 | 90% |
Reaction Steps
To a suspension of 2,3-dihydro-2,4,6,7-tetramethyl-2-[(4-phenyl-1-piperidinyl)methyl]-5-benzofuranamine dihydrochloride (1.3 g) in tetrahydrofuran (10 mL) was added a solution of sodium carbonate (0.95 g) in water (5 mL) with ice-cooling and the mixture was stirred for 5 minutes. Then, 0.26 mL of acetyl chloride was added dropwise and the mixture was stirred at room temperature for 15 minutes. This reaction mixture was diluted with water and extracted with 2 portions of ethyl acetate. The pooled organic layer was washed with water and saturated aqueous NaCl, dried over MgSO4, filtered, and concentrated under reduced pressure. The residue was crystallized from ethyl acetate/diisopropyl ether to provide 1.1 g of the title compound. Yield 90%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06172085B2 |
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| Source dataset | uspto-grants-2001_01 |
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| ORD ID | ord-188a81474bd7446186e6cfb55df2aae7 |
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| Source note | uspto-grants-2001_01 |
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