HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzene → 2-(Bromomethyl)-4-chloro-1-iodobenzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzene | HCID 241 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Phosphorus tribromide | HCID 24614 | — |
| Reactant | (5-Chloro-2-iodophenyl)methanol | HCID 818020 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 2-(Bromomethyl)-4-chloro-1-iodobenzene | HCID 9862384 | 247.4% |
Reaction Steps
A mixture of 41.6 g of phosphorus tribromide, 25 ml of benzene and 8.2 ml of pyridine is prepared while cooling and while stirring it is treated dropwise at a maximum temperature of 10° C. with 108.3 g of 5-chloro-2-iodobenzyl alcohol. Then, it is stirred for 4 hours at room temperature and for 1 hour at 50° C. After cooling, it is diluted with 120 ml of chloroform, the mixture washed with 25 ml of 5% hydrochloric acid, a 5% sodium hydroxide solution and with water, dried with magnesium sulfate and evaporated. There are obtained 126 g (95%) of crude 5-chloro-2-iodobenzyl bromide melting at 75°-79° C. The pure product is obtained by crystallization from a mixture of benzene and petroleum ether, m.p. 77°-79° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04431808 |
| Source dataset | uspto-grants-1984_02 |
| ORD ID | ord-56f5d6592a42441684f0adcd10d8f599 |
| Source note | uspto-grants-1984_02 |