HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 920897Generated: October 30, 2026
Phosphonium, (bromomethyl)triphenyl-, bromide (1:1) → HCID 86683114, compound
https://huagongshe.com/reaction/920897
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphonium, (bromomethyl)triphenyl-, bromide (1:1) | HCID 2733422 | — |
| Reactant | 3-Methylquinoline-2-carbaldehyde | HCID 22832126 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Diisopropyl Ether | HCID 7914 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86683114 | HCID 86683114 | 34% |
Reaction Steps
To a suspension of (bromomethyl)triphenylphosphonium bromide (3.06 g, 7.01 mmol) in 30 mL of THF, potassium tert-butoxide (0.78 g, 7.01 mmol) was added portionwise at −75° C. under argon. After completion of the addition, the mixture was stirred for 1 h a −75° C. Then, a solution of 3-methylquinoline-2-carbaldehyde (1 g, 5.84 mmol) in 20 mL of THF was added. The reaction mixture was stirred for 5 h at −75° C. and then allowed to warm up to room temperature overnight. For work-up, the reaction mixture was diluted with diisopropyl ether (1:1) and the precipitate formed was sucked off. The filtrate was concentrated and triturated in diisopropyl ether. The precipitate was sucked off. The filtrate was purified by column chromatography (normal phase, eluent: cyclohexane/EA) to give 492.5 mg (34%) of the title compound as yellow solid. LC-MS: m/e 248.0 (M+H)+; Rt 1.561 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09273068B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-38e962eaa58645c38ec34740b37ceaf0 |
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| Source note | uspto-grants-2016_03 |
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