HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1987159Generated: October 31, 2026
HCID 69079353, compound → HCID 69077265, compound
https://huagongshe.com/reaction/1987159
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 69079353 | HCID 69079353 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69077265 | HCID 69077265 | — |
Reaction Steps
Grignard Addition A solution of Boc-3-amino-4-phenyl-2-butanone (0.5 g, 1.9 mmol) in 100 mL methylene chloride was cooled to −78° C. and treated with methyl magnesium bromide (1.39 mL of a 3.0M solution, 4.2 mmol). The reaction was warmed to ambient temperature and stirred for 14 hours. The reaction was charged with additional methyl magnesium bromide (1.39 mL of a 3.0 M solution, 4.2 mmol) and stirred at ambient temperature for 5 hours. The reaction was quenched with ammonium chloride solution and partitioned between water and ethyl acetate. The organics were washed with water (3×), brine, dried over sodium sulfate, filtered and evaporated in vactio. Purification by flash column chromatography (20-35% ethyl acetate/hexanes) gave Boc-3-amino-2-methyl-4-phenylbutan-2-ol as a white solid: 1H NMR (400 MHz, CDCl3) δ 7.25 (m, 5H), 4.52 (m, 1H), 3.69 (m, 1H), 3.09 (dd, J=14.1, 3.3 Hz, 1H), 2.61 (t, J=12.0 Hz, 1H), 2.39 (s, 1H), 1.30 (m, 15H). Step B: Deprotection
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07550481B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-34fa0345be424c0e8738a27809120126 |
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| Source note | uspto-grants-2009_06 |
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