HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1927294Generated: October 31, 2026
Diethanolamine → (1R)-1-(2-bromo-3-methylphenyl)ethanol
https://huagongshe.com/reaction/1927294
Participants
| Role | Name | HCID | Charge |
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| Reactant | Diethanolamine | HCID 8113 | — |
| Reactant | Chlorobis((1S,2R,3S,5S)-2,6,6-trimethylbicyclo(3.1.1)hept-3-yl)borane | HCID 9923113 | — |
| Reactant | HCID 57514834 | HCID 57514834 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (1R)-1-(2-bromo-3-methylphenyl)ethanol | HCID 58572449 | 99% |
Reaction Steps
(+)-B-chlorodiisopinocampheylborane (8.46 g, 26.4 mmol) was dissolved in tetrahydrofuran (150 mL), cooled to −20° C., slowly added dropwise with a solution of 1-(2-bromo-3-methylphenyl)ethanone (4.30 g, 20.3 mmol) described in US 2007/167506 in tetrahydrofuran (50 mL), and stirred for 18 hours. The reaction solution was added with diethanolamine (6.38 g, 60.8 mmol), cooled to room temperature, and stirred at room temperature for 3 hours. The reaction solution was concentrated under reduced pressure and added with n-hexane (100 mL). The precipitated solids were filtered off and the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/ethyl acetate=4/1) to give the title compound as a white solid (4.30 g, yield 99%, 95.6% ee).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08183272B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-2deb15fdc08444289e13499f57b05116 |
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| Source note | uspto-grants-2012_05 |
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