Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2420646Generated: October 31, 2026

Hydrochloric Acid → 6-Fluoro-3-pentylchroman-7-carbaldehyde

https://huagongshe.com/reaction/2420646

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1-PiperidinecarboxaldehydeHCID 17429—
Reactant7-Bromo-6-fluoro-3-pentylchromanHCID 59288337—
ReactantButyllithiumHCID 178418339—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product6-Fluoro-3-pentylchroman-7-carbaldehydeHCID 59288351—

Reaction Steps

15.5 g (51.5 mmol) of 7-bromo-6-fluoro-3-pentylchroman are dissolved in 85 ml of THF, and 35 ml (55.7 mmol) of a 15 percent solution of n-butyllithium in n-hexane are slowly added at −70° C. After 1 h, 6.3 ml (56.7 mmol) of N-formylpiperidine in 15 ml of THF are added dropwise, and the mixture is stirred for 1 h. The batch is subsequently allowed to thaw, added to water, acidified using dil. hydrochloric acid and extracted three times with MTB ether. The combined org. phases are washed with water and sat. sodium chloride soln. and dried over sodium sulfate, the solvent is removed in vacuo, and the residue is recrystallised from heptane at −25° C., giving 6-fluoro-3-pentylchroman-7-carbaldehyde as colourless crystals (Rf=0.4; 1-chlorobutane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07955664B2
Source datasetuspto-grants-2011_06
ORD IDord-63485a51519049168b72d9ac649dbebd
Source noteuspto-grants-2011_06