HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 4-Nitrobenzothioamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 4-Nitrobenzamide | HCID 12091 | — |
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-Nitrobenzothioamide | HCID 3000564 | 119.3% |
Reaction Steps
6.06 g (15 mmol) of Lawesson reagent is added to a solution of 4.15 g (25 mmol) of 4-nitrobenzamide in 100 ml of 1,4-dioxan. The reaction mixture is heated under reflux for two hours. After the solution has returned to ambient temperature, it is poured into 150 ml of water and extracted with 5 times 100 ml of ethyl acetate. The organic solution is dried over magnesium sulphate, filtered and concentrated under vacuum in order to produce a yellow oil which is purified on a silica gel column (eluant: heptane/ethyl acetate 1/1). The pure fractions are collected and concentrated under vacuum. 3.26 g of a yellow powder is obtained with a yield of 72%. Melting point: 165-167° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06630461B2 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-2c4a48306fe446aebbb9f9c5ecc8818a |
| Source note | uspto-grants-2003_10 |