HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenyl-5-propyl-thiophene-2-carboxylic acid methoxy-methyl-amide → 1-(4-Phenyl-5-propyl-thiophen-2-yl)-ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenyl-5-propyl-thiophene-2-carboxylic acid methoxy-methyl-amide | HCID 86640176 | — |
| Reactant | HCID 178418573 | HCID 178418573 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(4-Phenyl-5-propyl-thiophen-2-yl)-ethanone | HCID 67165130 | — |
Reaction Steps
At 2° C. methylmagnesium bromide (1 mL, 1.7 M in THF) is added to a solution of 4-phenyl-5-propyl-thiophene-2-carboxylic acid methoxy-methyl-amide (900 mg, 3.11 mmol). The mixture stirred for 1 h before another portion (0.2 mL) of the Grignard reagent is added. Stirring is continued for 2 h. The mixture is diluted with water, extracted with EA and the organic extracts are dried over MgSO4 and concentrated. The crude product is purified by CC on silica gel eluting with heptane:EA 5:4 to give 1-(4-phenyl-5-propyl-thiophen-2-yl)-ethanone (456 mg) as a yellow oil; LC-MS: tR=1.06 min, [M+1]+=245.14, 1H NMR (CDCl3): δ 7.59 (s, 1H), 7.47-7.32 (m, 5H), 2.87-2.81 (m, 2H), 2.54 (s, 3H), 1.76-1.63 (m, 2H), 0.95 (t, J=/.6 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07951794B2 |
| Source dataset | uspto-grants-2011_05 |
| ORD ID | ord-7876e186fdaf45a286fdfbc5478001ef |
| Source note | uspto-grants-2011_05 |