HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,8-Diazabicyclo(5.4.0)undec-7-ene → Thiophene-2-carboxylic acid 2-trimethylsilanyl-ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | HCID 66751042 | HCID 66751042 | — |
| Reactant | HCID 67138806 | HCID 67138806 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Thiophene-2-carboxylic acid 2-trimethylsilanyl-ethyl ester | HCID 86591038 | — |
Reaction Steps
A solution of the title B compound in Example 9, 2-(2,4-dimethoxybenzyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one (7.00 g, 24.4 mmol) and DBU (3.71 g, 24.4 mmol) in CH2Cl2 (200 mL) is treated with the title B compound, 5-bromomethyl-thiophene-2-carboxylic acid 2-trimethylsilanyl-ethyl ester (8.25 g, 25.7 mmol). The mixture is stirred at RT for 3 h and the solvent is evaporated. The residue is chromatographed over silica gel using 20%-50% EtOAc in hexane as the eluent to afford 5-[5-(2,4-dimethoxy-benzyl)-1,1,4-trioxo-1,2,5]thiadiazolidin-2-ylmethyl]-thiophene-2-carboxylic acid 2-trimethylsilanyl-ethyl ester as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07291635B2 |
| Source dataset | uspto-grants-2007_11 |
| ORD ID | ord-7fefd366b0d84979a2237efd63dec5d3 |
| Source note | uspto-grants-2007_11 |