HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 359657Generated: October 29, 2026
Hydrochloric Acid → HCID 14496323, compound
https://huagongshe.com/reaction/359657
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 14496321 | HCID 14496321 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 14496323 | HCID 14496323 | 99% |
Reaction Steps
6.09 g (20 mmol) of (+)-4-benzyloxy-4'-(1-hydroxyethyl)biphenyl was dissolved in 100 ml of dry pyridine, followed by dropwise addition of 1.73 g (22 mmol) of acetyl chloride The mixture was stirred at room temperature for one hour, then poured into 1 liter of 2N hydrochloric acid and extracted with 300 ml of toluene. The toluene layer was washed with water, then with a 7% sodium bicarbonate solution and again with water successively in that order and then dried over anhydrous magnesium sulfate. This toluene solution was distilled under reduced pressure to remove the solvent and the residual white solid was purified by column chromatography packed with 200 g of silica gel to obtain 6.86 g of (+)-4-benzyloxy-4'-(1-acetoxyethyl)biphenyl in a 99% yield. It was further purified by recrystallization from ethanol. [α]D25 =+56.3° (c=1, CHCl3); melting point: 137° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05002693 |
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| Source dataset | uspto-grants-1991_03 |
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| ORD ID | ord-03f70c4b44fc4d439da630c3e100bbee |
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| Source note | uspto-grants-1991_03 |
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