HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 57431972, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethylthiocarbamoyl chloride | HCID 27871 | — |
| Reactant | Methyl 3-Hydroxyphenylacetate | HCID 39129 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57431972 | HCID 57431972 | — |
Reaction Steps
A mixture of (3-Hydroxy-phenyl)-acetic acid methyl ester (5.5 g, 33.1 mmol), N,N-dimethyl thiocarbamoyl chloride (5.11 g, 41.38 mmol), triethylamine (9.2 mL, 66.2 mmol), N,N-dimethylamino pyridine (0.4 g, 3.31 mmol) and dioxane (50 mL) is stirred at reflux 18 hr. The mixture is concentrated, partioned between 1M aqueous hydrochloric acid (200 mL) and ethyl acetate (3×75 mL). The combined organic extracts are dried over anhydrous magnesium sulfate, filtered, concentrated, and purified via silica chromatography eluting the product with dichloromethane to afford the title compound as a brown oil, 6.8 g, 81%. MS M++1 254. The structure is confirmed by 1H NMR spectroscopy.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07259175B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-ca90a9a4cf36445faf3a32252f3adb38 |
| Source note | uspto-grants-2007_08 |