HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Bisulfate → HCID 14473226, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 3-Bromo-4-butylthiophene | HCID 12502679 | — |
| Reactant | 3-Methoxy-4-butylthiophene | HCID 19099073 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | 1-Hexanol | HCID 8103 | — |
| Product | HCID 14473226 | HCID 14473226 | — |
Reaction Steps
10 g of 3-methoxy-4-butylthiophene, prepared from 3-bromo-4-butylthiophene by reaction with sodium methylate in methanol with catalysis by CuO, b.p. 54° C./0.26 mbar, were dissolved as in Example 14 in 50 cm3 of 1-hexanol and 30 ml of toluene, and 1 g of NaHSO4 was added. After distilling off 6 cm3 of azeotrope, the batch was worked up as in Example 14. Yield 8.5 g of 3-hexyloxy-4-butylthiophene of b.p. 112° to 116° C./0.26 mbar, which corresponds to 60% of theory.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04931568 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-fae56391e3174a5ba90dc7325230c000 |
| Source note | uspto-grants-1990_06 |