HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45448Generated: October 29, 2026
Ammonium Chloride → HCID 67103683, compound
https://huagongshe.com/reaction/45448
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | (2'-(Benzyloxy)-3'-tert-butylbiphenyl-3-yl)(pyridin-2-yl)methanone | HCID 67103457 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Catalyst | Methyltriphenyliphosphonium bromide | HCID 74505 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67103683 | HCID 67103683 | 16% |
Reaction Steps
A solution of methyltriphenylphosphoniumbromide (1.4 g, 3.9 mmol) in anhydrous tetrahydrofuran (15 mL) was stirred under nitrogen on an ice bath and 2.5 M n-butyllithium in hexanes (1.5 mL, 3.75 mmol) was slowly added. After 20 min. the cold bath was removed and stirring was continued at room temperature for 1 hr. The reaction mixture was cooled on an ice bath and a solution of 11 (0.82 g, 1.95 mmol) in tetrahydrofuran (15 mL) was added at such a rate that the temperature did not exceed 5° C. Stirring was continued overnight at room temperature. The reaction mixture was poured on saturated ammonium chloride (120 mL) and extracted with ethyl acetate (150 mL). The organic extract was washed with water (2×80 mL), dried over sodium sulfate and stripped. The residue was purified by chromatography on silica (50 g) with 5% ethyl acetate in heptane (3 L) to produce pure 12 (0.13 g, 16%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541522B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-6796b4a070e94148a0d9de33d169279a |
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| Source note | uspto-grants-2013_09 |
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