HuagongsheHuagongshe Chemistry Print Report · For research reference only
Trifluoroacetic acid → [2-(Ethoxycarbonyl)-1-benzothien-6-yl]malonic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Di-tert-butyl [2-(ethoxycarbonyl)-1-benzothien-6-yl]malonate | HCID 59424236 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | [2-(Ethoxycarbonyl)-1-benzothien-6-yl]malonic acid | HCID 59424242 | — |
Reaction Steps
Di-tert-butyl[2-(ethoxycarbonyl)-1-benzothien-6-yl]malonate (0.873 g, 2.08 mmol) was dissolved in DCM (5 mL) and TFA (5 mL) was added. The solution was stirred at room temperature for 2 hours. The solvent was removed in vacuo and the residue partitioned between saturated NaHCO3-EtOAc. The aqueous phase was acidified with 2N HCl and extracted with EtOAc. The combined organic extracts were dried over MgSO4 and concentrated in vacuo to give the product (white solid). 1H NMR (DMSO-d6) δ 13.10 (br s, 2H), 8.17 (s, 1H), 8.03 (s, 1H), 7.98 (d, J=8.4 Hz, 1H), 7.47 (dd, J=8.4, 1.8 Hz, 1H), 4.83 (s, 1H), 4.33 (q, J=7.2 Hz, 2H), 1.32 (t, J=7.2 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07834034B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-8067dd964e7242a0977b5bc68225919a |
| Source note | uspto-grants-2010_11 |