HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968441Generated: October 29, 2026
4-Hydroxybenzaldehyde → HCID 23397582, compound
https://huagongshe.com/reaction/968441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Hydroxybenzaldehyde | HCID 126 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,3,4-Tri-O-acetyl-alpha-D-xylopyranosyl bromide | HCID 11013202 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 23397582 | HCID 23397582 | — |
Reaction Steps
p-Hydroxybenzaldehyde (2.2 g, 18 mmol), dichloromethane (20 mL) and a 5% aqueous solution of sodium hydroxide (25 mL) were put in a 100 mL round bottom flask and stirred vigorously. At that time, a water phase turned yellow. To the resulting mixture, tetrabutylammonium bromide (1.0 g, 3.0 mmol) was added, and then, a dichloromethane (about 6 mL) solution of 2,3,4-tri-O-acetyl-α-D-xylopyranosyl bromide (4.0 g, 12 mmol) was added dropwise. A reaction vessel was protected from light. The resulting mixture was stirred vigorously at room temperature for 2 days. The separated organic phase was washed with 50 mL of a 5% aqueous solution of sodium hydroxide three times and then with 50 mL of water three times, dried over anhydrous sodium sulfate and evaporated to dryness to give the title compound. Light brown solid. Yield 1.5 g, 34%. The product was unstable at room temperature, and stored in the freezer.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06958389B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-eb16844ebd1546b9897f4b2dcf002900 |
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| Source note | uspto-grants-2005_10 |
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