HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 13210860, compound → HCID 13210862, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 13210860 | HCID 13210860 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Product | HCID 13210862 | HCID 13210862 | 76% |
Reaction Steps
The 1-benzyloxy-2-chloro-4-(2-phenethyloxyethoxy)-benzene obtained according to the preceding paragraph was stirred in 20 ml of 48% hydrogen bromide in glacial acetic acid at 25° C. for 30 minutes. The solution was evaporated to dryness and the residue was partitioned between 2N aqueous sodium hydroxide and diethyl ether. The aqueous phase was acidified to pH 6 with concentrated hydrochloric acid and extracted with ethyl acetate. The organic extract was washed with water, dried over sodium sulfate, filtered and evaporated to give 2.06 g (76%) of 2-chloro-4-(2-phenethyloxyethoxy)phenol in the form of an oil which was homogeneous according to chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04649160 |
| Source dataset | uspto-grants-1987_03 |
| ORD ID | ord-9c42c10bba0144f7ae878233e3deb12e |
| Source note | uspto-grants-1987_03 |