HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1826686Generated: October 31, 2026
Pentane → (2-Aminophenyl)(3-methoxyphenyl)methanone
https://huagongshe.com/reaction/1826686
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pentane | HCID 8003 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 2-Bromoanisole | HCID 11358 | — |
| Reactant | 2-Aminobenzonitrile | HCID 72913 | — |
| Reactant | HCID 178418306 | HCID 178418306 | — |
| Product | (2-Aminophenyl)(3-methoxyphenyl)methanone | HCID 22135242 | 14% |
Reaction Steps
To a solution of bromoanisole 91 (1.38 mL, 10.7 mmol) in THF (5 mL) at 78° C. and under nitrogen atmosphere, was added 1.2 M t-BuLi in pentane (18.2 mL, 21.9 mmol) dropwise. After stirring for 20 min, anthranilonitrile 92 (0.63 g, 5.3 mmol) was added. The reaction was warmed to rt and stirred overnight. The reaction was cooled to 0° C. and quenched with 3N HCl. After stirring 30 min at rt, the acidic extracts were washed with EtOAc (3×12 mL). The aqueous layer was made basic (pH>10) using 6N NaOH and extracted with CH2Cl2. The organic extracts were washed with sat. NaCl, dried over NaSO4, filtered, and concentrated to give a crude mixture containing 93. The crude oil was purified by chromatography on silica to provide pure 93 (0.17 g, 14%) as a yellow oil; 1H NMR (500 MHz, DMSO-d6) δ 7.40–7.43 (m, 1H), 7.27–7.30 (m, 1H), 7.07–7.17 (m, 4H), 6.86–6.88 (m, 1H), 6.49–6.52 (m, 1H), 3.81 (s, 3H); CI MS m/z=228 [C14H13NO2+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07053084B1 |
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| Source dataset | uspto-grants-2006_05 |
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| ORD ID | ord-5c14dd280f9a452e821bc266bfcbaaa4 |
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| Source note | uspto-grants-2006_05 |
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