HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 352287Generated: October 29, 2026
Hydrogen Bromide → HCID 12905063, compound
https://huagongshe.com/reaction/352287
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86588768 | HCID 86588768 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Product | HCID 12905063 | HCID 12905063 | — |
Reaction Steps
2,3,4,6-tetra-O-benzyl-D-galactopyranosylacetate (79.8 g) was dissolved in a mixture of toluene (160 ml) and isopropyl ether (520 ml), and the solution was cooled to −10 to 0° C. To this solution, an isopropyl ether solution (2.8 mmol/ml, about 100 ml) containing 2.0 equivalent volumes of HBr was added. After stirring for about 90 minutes at −10 to 0° C., an aqueous 5% sodium hydrogencarbonate solution was poured into the reaction solution, and excessive HBr was neutralized by stirring. The whole volume was transferred into a separation funnel for separation, then the water layer was discarded and washing was carried 2 times with an aqueous 10% sodium chloride solution. After concentration under vacuum, 2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl bromide (GalBr) was obtained as a syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06747010B2 |
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| Source dataset | uspto-grants-2004_06 |
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| ORD ID | ord-39e3d943c78e44f3b56b3000bef97ae2 |
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| Source note | uspto-grants-2004_06 |
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