HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 652722Generated: October 30, 2026
Hydrochloric Acid → 6-(p-Chlorophenyl)hexylamine
https://huagongshe.com/reaction/652722
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | p-Chlorophenyl hexanamide | HCID 25149977 | — |
| Reactant | Diborane tetrahydrofuran | HCID 131714434 | — |
| Product | 6-(p-Chlorophenyl)hexylamine | HCID 13535795 | 67% |
Reaction Steps
A solution of 16.4 g (0.073 mole) of 6-(p-chlorophenyl hexanamide (VI) in 30 ml. of dry tetrahydrofuran was added dropwise to a stirred solution of 170 ml of 1.0M diborane/tetrahydrofuran solution (Aldrich) at 0° C. under a nitrogen atmosphere. After addition, the mixture was stirred at 0° C. for 15 minutes, then warmed to reflux and kept there for 2.5 hours. The mixture was cooled to room temperature, and 85 ml of 6N hydrochloric acid was added cautiously to quench the reaction. The solvent was removed and the aqueous mixture was brought to pH 10 with 10% sodium hydroxide solution. The aqueous mixture was extracted three times with 60 ml portions of ethyl acetate. The combined ethyl acetate extracts were washed with saturated sodium chloride solution, dried over sodium sulfate, filtered, and evaporated leaving an oil. Distillation under reduced pressure afforded 10.4 g (67%) of VII as a colorless oil, bp. 108°-115° C. (0.3 torr).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04673677 |
|---|
| Source dataset | uspto-grants-1987_06 |
|---|
| ORD ID | ord-181f2120a30e4aa4b6254a6b87db4bec |
|---|
| Source note | uspto-grants-1987_06 |
|---|