HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1522951Generated: November 2, 2026
Water → 1-(((S)-2-(Bromomethyl)-3-methylbutoxy)methyl)benzene
https://huagongshe.com/reaction/1522951
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Phosphorus oxybromide | HCID 24613 | — |
| Reactant | (R)-2-(benzyloxymethyl)-3-methylbutan-1-ol | HCID 68782329 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(((S)-2-(Bromomethyl)-3-methylbutoxy)methyl)benzene | HCID 11715991 | 81.6% |
Reaction Steps
Dissolve (R)-2-(benzyloxy-methyl)-3-methyl butanol (15.6 g, 75 mmol) in N,N-dimethyl formamide (246 ml), add phosphorus oxybromide (22.58 g, 78.75 mmol) in droplets slowly and control the temperature below 50° C. in that process, and then let them to react at 50° C. for 3 hours. Cool down to room temperature, and pour the reactant liquid into water (246 ml) slowly, extract with normal hexane for three cycles, combine the normal hexane layers, wash twice with saturated sodium bicarbonate and saturated sodium chloride respectively, dry the organic layer with anhydrous sodium sulfate, filter, and condense the filtrate so as to obtain 18.1 g of oily matter. Treat the oil matter by reduced pressure distillation to obtain 16.6 g of colorless transparent liquid; the yield is 81.1%, and the chiral purity is ≧99.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09079839B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-dd6fbddcd20641879102440530630273 |
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| Source note | uspto-grants-2015_07 |
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