HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1009294Generated: October 31, 2026
1,4-Dibromobenzene → HCID 57446955, compound
https://huagongshe.com/reaction/1009294
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,4-Dibromobenzene | HCID 7804 | — |
| Reactant | Cyclohexane | HCID 8078 | — |
| Reactant | HCID 57515780 | HCID 57515780 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 57446955 | HCID 57446955 | — |
Reaction Steps
Butyllithium (41 mL of a 2.0M cyclohexane solution) was added at −30° C. to a solution of 1,4-dibromobenzene (19.3 g, 81.89 mmol) in ether (250 mL) over 10 minutes. After 1 hour, a solution of (4S)-4-propyl-2-trifluoromethyloxazolidine (3.00 g, 16.38 mmol) was added in ether (50 mL) over 30 minutes via an addition funnel. After 90 minutes of stirring, water (100 mL) was added. The organic phase was washed with brine (100 mL), dried over MgSO4, filtered, and evaporated to dryness. The residue was purified on a plug of silica gel (10-30% ethyl acetate/hexane elution). An approximately 2:1 mixture of diastomers of (2S)-2-[1-(4-bromophenyl)-2,2,2-trifluoroethylamino]-pentan-1-ol at the CF3 residue was observed based on the norvaline methyl triplet at 0.98 ppm (1H NMR).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07973037B2 |
|---|
| Source dataset | uspto-grants-2011_07 |
|---|
| ORD ID | ord-ce1a741ee4664d5d93cbf361d34aaac7 |
|---|
| Source note | uspto-grants-2011_07 |
|---|