HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → 3-(5-Fluorobenzothiazol-2-ylmethoxy)benzyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 3-(5-Fluorobenzothiazol-2-ylmethoxy)benzyl alcohol | HCID 53637583 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-(5-Fluorobenzothiazol-2-ylmethoxy)benzyl bromide | HCID 19019471 | 71.9% |
Reaction Steps
To a solution of 1.04 g of 3-(5-fluorobenzothiazol-2-ylmethoxy)benzyl alcohol (Preparation L) in 60 ml of dry tetrahydrofuran was added 2.38 g of carbontetrabromide and 1.89 g of triphenylphosphine and the reaction stirred under nitrogen at room temperature for 1.5 hours. The reaction mixture was filtered, treated with 100 ml of water and extracted with ethyl acetate. The extracts were washed with water and a brine solution and dried over sodium sulfate. The solvent was removed and the residual brown solid chromatographed on 200 g of silica gel using from 5-10% ethyl acetate--95-90% hexane (v:v). The fractions containing the product were combined and concentrated to give 910 mg of the titled product, m.p. 99°-100° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05322847 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-08744490abca494ba1deba0146110a81 |
| Source note | uspto-grants-1994_06 |