HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2087151Generated: October 30, 2026
Diethyl Ether → (+)-β-Amino-3,4-difluoro-α,α-dimethylbenzeneethanol
https://huagongshe.com/reaction/2087151
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Methyl 2-aMino-2-(3,4-difluorophenyl)acetate | HCID 22049608 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Product | (+)-β-Amino-3,4-difluoro-α,α-dimethylbenzeneethanol | HCID 18623229 | 62% |
Reaction Steps
Into a well-stirred solution of methyl 2-amino-2-(3,4-difluorophenyl)acetate (10.5 g, 52.19 mmol) in anhydrous ether (200 mL) at 0° C. a solution of methylmagnesium bromide (3 M, 87 mL, 261 mmol) in ether was added over 10 minutes. The reaction mixture was stirred at 0° C. for 2.5 h and allowed to warm to room temperature. After 12 h, the reaction mixture was carefully poured onto a mixture of ice (300 g) and saturated aqueous ammonium chloride (50 9). The ether layer was separated and the aqueous layer was extracted with more ether (4×200 mL). The combined extracts were dried with magnesium sulfate and the solvent evaporated. The crude product was purified by column chromatography on silica gel using chloroform/methanol/2M ammonia in methanol (1000:20:10, 1000:40:20, 1000:80:40) as the eluent to give the product as an oil (6.5 g, 62% yield) which was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06727264B1 |
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| Source dataset | uspto-grants-2004_04 |
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| ORD ID | ord-46409637879847edbb63caef28e3db96 |
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| Source note | uspto-grants-2004_04 |
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