HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetone → Methyl 3-[2-(acetylsulfanyl)acetamido]benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetone | HCID 180 | — |
| Reactant | methyl 3-[(chloroacetyl)amino]benzoate | HCID 2304955 | — |
| Reactant | Potassium 2-thienylacetate | HCID 23696799 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | Methyl 3-[2-(acetylsulfanyl)acetamido]benzoate | HCID 20382891 | — |
Reaction Steps
A mixture of methyl 3-(2-chloroacetamido)benzoate (16 g., 0.07 mole) and potassium thiolacetate (7.1 g., 0.065 mole) in 150 ml. of acetone is refluxed for 4.5 hr. After cooling, the reaction mixture is filtered and the filtrate concentrated under reduced pressure. The residual solid thus obtained is slurried with n-hexane to afford an 86% yield of crude product. Crystallization of the crude product from ethyl acetate-n-hexane affords analytically pure METHYL 3-[2-(ACETYLTHIO)ACETAMIDO]BENZOATE, m.p. 117.5°-119.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04096277 |
| Source dataset | uspto-grants-1978_06 |
| ORD ID | ord-7d475b2e85cb4ee6a37befc20f1046a7 |
| Source note | uspto-grants-1978_06 |