HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Bromide → 7-Bromo-6-hydroxy-1-heptanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Bromide | HCID 253877 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 5-(Oxiran-2-yl)pentan-1-ol | HCID 13616673 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetic acid tetrahydrofuran | HCID 23444217 | — |
| Product | 7-Bromo-6-hydroxy-1-heptanol | HCID 13366074 | — |
Reaction Steps
A mixture of 5 (120 mg, 0.9 mmol) in acetic acid-tetrahydrofuran (2 mL-0.4 mL) was treated with 0.3 mL of saturated aqueous potassium bromide solution at room temperature over 67 hours. It was then diluted with ether and poured into saturated aqueous sodium bicarbonate. The separated organic layer was washed with saturated sodium thiosulfite, saturated sodium chloride, and dried over magnesium sulfate. Evaporation of the solvent gave 127 mg of 7-bromo-6-hydroxy-1-heptanol (4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04456613 |
| Source dataset | uspto-grants-1984_06 |
| ORD ID | ord-e55ae0ea8bc44e1187f5e1d9052070fc |
| Source note | uspto-grants-1984_06 |