HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-{[(4-Hydroxyphenyl)thio]methyl}benzaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Mercaptophenol | HCID 240147 | — |
| Reactant | 4-(Bromomethyl)benzaldehyde | HCID 11206421 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-{[(4-Hydroxyphenyl)thio]methyl}benzaldehyde | HCID 57859823 | 62% |
Reaction Steps
A solution of 4-bromomethylbenzaldehyde (0.3 g, 1.5 mmol) and 4-hydroxythiophenol (0.2 g, 1.5 mmol) in 1,4-dioxane (10 mL) was degassed and treated with triethylamine (0.44 mL, 3.11 mmol). After stirring for 1 day the mixture was diluted with water (20 mL) and extracted with ethyl acetate (2-fold 20 mL). The combined organic extracts were washed with brine and dried (sodium sulphate) and the solvent removed in vacuo. The crude material was purified by flash column chromatography on silica gel eluting with heptane:ethyl acetate (9:1 changing to 0:1, by volume) to give the title compound as a solid, 62% yield, 220 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08822439B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-27e1a94d734546d89f486bedceb60609 |
| Source note | uspto-grants-2014_09 |