HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-(Benzo[b]thiophen-3-yl)-2-oxopropyl Acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3-(3,4-Dichlorophenyl)-2-oxopropyl Acetate | HCID 16100072 | — |
| Reactant | 1-(Benzo[b]thiophen-3-yl)-3-chloropropan-2-one | HCID 16100179 | — |
| Product | 3-(Benzo[b]thiophen-3-yl)-2-oxopropyl Acetate | HCID 16100076 | 51% |
Reaction Steps
The procedure described above for the synthesis of 3-(3,4-dichlorophenyl)-2-oxopropyl acetate was followed, reacting 1-(benzo[b]thiophen-3-yl)-3-chloropropan-2-one (0.661 g, 2.94 mmol) with acetic acid (0.34 mL, 0.35 g, 5.9 mmol) and triethylamine (0.82 mL, 0.59 g, 5.9 mmol). Flash chromatography over silica gel (10-40% ethyl acetate in hexanes) gave pure product (0.372 g, 51% yield): 1H NMR (400 MHz, CDCl3) δ 2.14 (s, 3H) 3.98 (s, 2H) 4.71 (s, 2H) 7.34-7.44 (m, 3H) 7.67-7.70 (m, 1H) 7.86-7.89 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07465798B2 |
| Source dataset | uspto-grants-2008_12 |
| ORD ID | ord-d55c715090c14942861801e3160916e6 |
| Source note | uspto-grants-2008_12 |