HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 658335Generated: October 29, 2026
Benzophenone → 3-tert-Butoxy-5-fluoroaniline
https://huagongshe.com/reaction/658335
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzophenone | HCID 3102 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Reactant | Binap, (A+-)- | HCID 634876 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1-Bromo-3-tert-butoxy-5-fluorobenzene | HCID 56844292 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-tert-Butoxy-5-fluoroaniline | HCID 66743914 | — |
Reaction Steps
1-Bromo-3-tert-butoxy-5-fluorobenzene (56.1 g), benzophenone (50.9 g), NaOMe (50.5 g) and 2,2′-Bis-diphenylphosphanyl-[1,1′]binaphthalenyl (17.5 g) are dissolved in toluene (500 ml). The reaction mixture is flushed with argon, Pd2(dba)3 (5.4 g) is added and the reaction mixture is heated to 80° C. for 40 hours. The reaction mixture is quenched with water. The organics are separated, dried over MgSO4, filtered and the solvent removed in vacuo. The intermediate is obtained by flash column chromatography (silica, eluent dichloromethane). The resulting product is then dissolved in MeOH (1 L). NaOAc (46.1 g), hydroxylamine hydrochloride (29.1 g) are added and the reaction mixture is stirred at room temperature for 2.5 hours. The reaction mixture is quenched with 0.1M NaOH, extracted into DCM (2×), dried over MgSO4, filtered and the solvent removed in vacuo to give the title compound. 1H nmr (CDCl3, 400 MHz); 6.20 (m, 3H), 3.75 (br s, 2H), 1.4 (s, 9H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08076489B2 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-b39c6c4777ea4c5a9cb839923abbe3c1 |
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| Source note | uspto-grants-2011_12 |
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