HuagongsheHuagongshe Chemistry Print Report · For research reference only
Stannane, [2,2'-bithiophen]-5-yltributyl- → 4-Formyl-5-hydroxymethyl-2,2':5', 2"-terthiophene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Stannane, [2,2'-bithiophen]-5-yltributyl- | HCID 11201877 | — |
| Reactant | 2-(Hydroxymethyl)-5-iodothiophene-3-carbaldehyde | HCID 18928889 | — |
| Catalyst | Dichlorobis(triphenylphosphine)palladium | HCID 6102075 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Formyl-5-hydroxymethyl-2,2':5', 2"-terthiophene | HCID 57321364 | 38% |
Reaction Steps
In a two-necked round bottomed flask was added 5-tributylstannyl-2,2'-bithiophene (2.04 g), bis(triphenylphosphine)palladium (II) chloride (0.19 g), 3-formyl-2-hydroxymethyl-5-iodo-thiophene (1.0 g) and tetrahydrofuran (20 ml). The reaction mixture was refluxed for 16 hours. Extracted with ethyl acetate, washed with brine, dried over anhydrous magnesium sulfate and concentrated. The residue was separated by silica gel chromatography, eluted with n-hexane/ethyl acetate (9:1→1:1 gradient) to give brownish solid product (0.43 g, 38%), melting point 108°-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05741811 |
| Source dataset | uspto-grants-1998_04 |
| ORD ID | ord-39c20772fcec42f3b22ab542dcb257ec |
| Source note | uspto-grants-1998_04 |