HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361506Generated: November 1, 2026
Hydrogen Bromide → HCID 23287941, compound
https://huagongshe.com/reaction/361506
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 15885495 | HCID 15885495 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 23287941 | HCID 23287941 | — |
Reaction Steps
1-(10,11-Dihydroxyundecanyl)-3,7-dimethylxanthine (3.6 g, 10 mmol) was stirred with hydrogen bromide (6.2 mL, 8.4 g of a 30% solution in acetic acid, 31.1 mmol) for 90 minutes. The mixture was then added to a flask containing 100 mL aqueous sodium bicarbonate solution and 75 mL dichloromethane. After 10 minutes of vigorous stirring the layers were separated and the aqueous portion washed with dichloromethane (3×75 mnL). The organic portions were combined, dried over magnesium sulfate, and evaporated to give 1-(10-acetoxy-11-bromoundecanyl)-3,7-dimethylxanthine (3.6 g). Without further purification, the bromoacetate was taken up in methanol (25 mL) and treated with a solution of sodium methoxide (prepared from 0.28 g, 12.2 mmol sodium, and 25 mL methanol). After 30 minutes, most of the solvent was removed under reduced pressure and the residue extracted with dichloromethane (3×75 mL). The organic portions were combined, dried over magnesium sulfate and concentrated under reduced pressure to obtain an off-white solid which was purified by column chromatography over silica gel using dichloromethane/(3%) methanol eluant to yield 2.0 g (57% yield) 1-(10,11-Oxidoundecanyl)-3,7-dimethylxanthine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05866576 |
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| Source dataset | uspto-grants-1999_02 |
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| ORD ID | ord-25cc4cedf2e24e418eace799319058e6 |
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| Source note | uspto-grants-1999_02 |
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