HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-[3,4-Bis(tert-butyldimethylsilanyloxy-methyl)phenoxymethyl]-5-((e)-4,4-dibromo-1-ethylbuta-1,3-dienyl)thiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Carbon tetrabromide | HCID 11205 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 88011784 | HCID 88011784 | — |
| Catalyst | Zinc | HCID 23994 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-[3,4-Bis(tert-butyldimethylsilanyloxy-methyl)phenoxymethyl]-5-((e)-4,4-dibromo-1-ethylbuta-1,3-dienyl)thiophene | HCID 88011451 | — |
Reaction Steps
770 mg (11.7 mmol) of zinc, 3.09 g (11.7 mmol) of triphenylphosphine and 3.9 g (11.7 mmol) of carbon tetrabromide are stirred for 30 minutes at room temperature in 150 mol of dichloromethane. A solution of 3.3 g (5.9 mmol) of (E)-3-{5-[3,4-bis(tert-butyldimethylsilanyloxymethyl)phenoxymethyl]-2-thienyl}pent-2-enal (described in Example 7(c)) in 30 mL of dichloromethane is then added dropwise. After stirring for 1 h at room temperature the reaction medium is treated with water and extracted with dichloromethane. After purification on silica gel (eluent: 95 heptane/5 ethyl acetate), the desired product is obtained in the form of a brown oil (m=3.9 g; Y=93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06706725B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-99c6d6addb954087a7bd32ee8fc34244 |
| Source note | uspto-grants-2004_03 |