HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-(4-Formylphenoxy)thiophene-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-(4-Formylphenoxy)thiophene-2-carbonitrile | HCID 58677373 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 5-(4-Formylphenoxy)thiophene-2-carboxamide | HCID 58677391 | — |
Reaction Steps
Dissolve 5-(4-formylphenoxy)thiophene-2-carbonitrile (0.818 g, 3.57 mmol) in DMSO (18 mL) in a round bottom flask, then add K2CO3 (0.247 g, 1.78 mmol). Cool the reaction flask in a water bath and add 30% H2O, (0.81 mL, 7.14 mmol) solution. After one hour, add water (25 mL). Filter the resulting precipitate and wash the filter cake with water (25 mL). Collect the filter cake as the title compound: HRMS calcd for C12H10NO3S 248.0381 (M+H)+, found 248.0396, time 0.36 min; HPLC [YMC-Pro pack C-18 (150×4.6 mm, S-5 microm), 0.05% TFA/acetonitrile in 0.05% TFA/water at 1.0 mL/min, 10-20% over 5 min, 20-95% over 18], tR=13.0 min, 100% purity.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07396943B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-c37712cba5734d42ae0f99e4f874d7bb |
| Source note | uspto-grants-2008_07 |