HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Methyl 3-thienylacetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 3-Thiophenacetic acid | HCID 23404 | — |
| Product | Methyl 3-thienylacetate | HCID 94041 | — |
Reaction Steps
To 2-(thiophen-3-yl)acetic acid in MeOH at 0° C. was added TMS-CH2N2. The solution was stirred for 3 hours then quenched with a few drops of AcOH. The solvents were evaporated. Column chromatography (SiO2, 3-15% EtOAc/Hex) gave pure methyl 2-(thiophen-3-yl)acetate (E41).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08153656B2 |
| Source dataset | uspto-grants-2012_04 |
| ORD ID | ord-ece1f5a62cc24514bcbe8ae5796bac21 |
| Source note | uspto-grants-2012_04 |