HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon tetrabromide → HCID 66846510, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 4176130 | HCID 4176130 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66846510 | HCID 66846510 | 86% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of 6-(triphenylmethoxymethyl)pyridine-2-methanol (16.8 g, 44 mmol) in CH2Cl2 at 0° C. was treated with triphenylphosphine (17.3 g, 66 mmol) and carbon tetrabromide (17.5 g, 52.8 mmol), stirred at 0° C. for 2.5 h then concentrated in vacuo to approximately a quarter of the original volume. The resulting solution was filtered through a pad of silica, washed with hexane:EtOAc (1:1) and the filtrate concentrated in vacuo to give the title compound (16.8 g, 86%) as a cream solid; NMR δH (400 MHz, DMSO) 4.14 (2H, s), 4.61 (2H, s), 7.27-7.48 (16H, m), 7.68 (1H, d, J 7.5 Hz) and 7.90 (1H, t, J 7.5 Hz); Rf (Hexane:EtOAc (2:1))=0.84
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07875600B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-aec5cdc4cccb4a01ada06e6469a66e35 |
| Source note | uspto-grants-2011_01 |