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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphonium, (bromomethyl)triphenyl-, bromide (1:1)HCID 2733422—
Reactant3-Methylquinoline-2-carbaldehydeHCID 22832126—
ReactantPotassium tert-butoxideHCID 23665647—
SolventDiisopropyl EtherHCID 7914—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86683114HCID 8668311434%

Reaction Conditions

Temperature-75 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273068B2
Source datasetuspto-grants-2016_03
ORD IDord-38e962eaa58645c38ec34740b37ceaf0
Source noteuspto-grants-2016_03