HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866851Generated: November 2, 2026
Hydrochloric Acid → 2-Phenylbicyclo[2.2.1]heptan-2-ol
https://huagongshe.com/reaction/1866851
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Bicyclo(2.2.1)heptan-2-one | HCID 10345 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-Phenylbicyclo[2.2.1]heptan-2-ol | HCID 417191 | — |
Reaction Steps
To a solution of norcamphor (60.0 g, 0.54 mole) in THF (1 L) at −65° C. was added phenyl magnesium bromide (200 mL of a 3 M solution in ether, 0.60 mole). The temperature was kept between −65° C. and −20° C. during the addition. After completion of addition, the mixture was slowly warmed to room temperature and stirred overnight. The mixture was cooled to 0° C. and saturated aqueous ammonium chloride (200 mL) was added carefully. A solution of 1 N hydrochloric acid was added until the residual salts were dissolved. The mixture was then extracted twice with ether and the combined organic phases were washed successively with water and brine. The organic layer was dried (MgSO4) and concentrated. Flash chromatography of the residue (silica gel; hexane/EtOAc 9:1) provided I-2a as a white solid (95.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07629467B2 |
|---|
| Source dataset | uspto-grants-2009_12 |
|---|
| ORD ID | ord-72bb5ddb236a4a8d851005f855986c26 |
|---|
| Source note | uspto-grants-2009_12 |
|---|