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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-Piperidinecarboxaldehyde | HCID 17429 | — |
| Reactant | 7-Bromo-6-fluoro-3-pentylchroman | HCID 59288337 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | 6-Fluoro-3-pentylchroman-7-carbaldehyde | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07955664B2 |
|---|
| Source dataset | uspto-grants-2011_06 |
|---|
| ORD ID | ord-63485a51519049168b72d9ac649dbebd |
|---|
| Source note | uspto-grants-2011_06 |
|---|