HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → Benzene, ((2-bromoethoxy)methyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-(Benzyloxy) ethanol | HCID 12141 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Benzene, ((2-bromoethoxy)methyl)- | HCID 73833 | 85% |
Reaction Steps
A solution of triphenyl phosphine (2.1 g, 7.9 mmol) in dry methylene chloride (16 mL) was added dropwise over 10 min to a stirred mixture of N-bromosuccinimide (1.4 g, 7.9 mmol) in dry methylene chloride (23 mL) at -78° C. The reaction was kept in the dark and stirring was continued until all the N-bromosuccinimide had dissolved (10 min). A solution of 2-(benzyloxy)ethanol in dry methylene chloride (10 mL) was added dropwise. The cooling bath was removed and stirring was continued for 12 h at rt. The organic layer was then concentrated in vacuo and passed through a silica plug with 1:1 hexane:methylene chloride to afford 2-(benzyloxy)bromoethane (1.20 g, 85%). ##STR185## Step 3
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05789434 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-04e3d4c7e2da4c678101e425a60464c9 |
| Source note | uspto-grants-1998_08 |