HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 580015Generated: November 1, 2026
Boron tribromide → HCID 20135527, compound
https://huagongshe.com/reaction/580015
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | HCID 20135524 | HCID 20135524 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 20135527 | HCID 20135527 | — |
Reaction Steps
Boron tribromide (0.66 ml. of a molar solution in methylene chloride) was added to a stirred solution of the (1RS,2RS)-2-p-fluorophenyl-1-(10-hexylthiodecyl)-1,2,3,4-tetrahydro-6-methoxynaphthalene thus obtained (0.11 g.) in methylene chloride (4 ml.) which was cooled to -70° C., and the mixture was allowed to warm up to laboratory temperature, stirred at that temperature for 16 hours and then poured onto ice (20 g.). The mixture was extracted three times with methylene chloride (10 ml. each time) and the combined extracts were washed with saturated aqueous sodium bicarbonate solution (5 ml.) and then with water, dried and evaporated to dryness. The residue was purified by chromatography on a silica gel column using toluene as eluent. There was thus obtained as an oil (1RS,2RS)-2-p-fluorophenyl-1-(10-hexylthiodecyl)-1,2,3,4-tetrahydronaphth-6-ol, the structure of which was confirmed by proton magnetic resonance and mass spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04751240 |
|---|
| Source dataset | uspto-grants-1988_06 |
|---|
| ORD ID | ord-26169348ae9b4460b2fc86e8433c5e7e |
|---|
| Source note | uspto-grants-1988_06 |
|---|