HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethyl Sulfide → [4-Iodo-3-(naphthalen-2-yloxy)-phenyl]-methyl bromide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethyl Sulfide | HCID 1068 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | [4-Iodo-3-(naphthalen-2-yloxy)-phenyl]-methanol | HCID 21697102 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [4-Iodo-3-(naphthalen-2-yloxy)-phenyl]-methyl bromide | HCID 21696995 | — |
Reaction Steps
To a solution of [4-iodo-3-(naphthalen-2-yloxy)-phenyl]-methanol (0.085 g, 0.226 mmol) in CH2Cl2 (2 mL) at −15° C. was added a cold (0° C.) solution of N-bromosuccinimide (0.120 g, 0.68 mmol) in dimethyl sulfide (0.060 mL, 0.814 mmol) with stirring. The reaction mixture was allowed to warm to ambient temperature overnight, concentrated to dryness, and chromatographed (SiO2, 10% EtOAc:hexane) to give the title compound which was used without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06297239B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-1d0e4b4c1d104fe6bc6b9e173c13e015 |
| Source note | uspto-grants-2001_10 |