HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Indanylacetic acid → 3-(2-indanylacetyl)-L-thioproline ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Indanylacetic acid | HCID 96501 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | Ethyl (4R)-4-thiazolidinecarboxylate | HCID 13011878 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(2-indanylacetyl)-L-thioproline ethyl ester | HCID 131716917 | 57.1% |
Reaction Steps
1.4 g of 2-indanylacetic acid and 1.9 g of WSC.HCl were added to 15 ml of methylene chloride under ice-cooling. The mixture was stirred for 5 minutes at room temperature. After an addition of 1.3 g of L-thioproline ethyl ester dissolved in 10 ml of methylene chloride, the mixture was stirred for 5 hours. The reaction mixture was washed with water, diluted hydrochloric acid, and saturated sodium hydrogen carbonate in this order. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue thus obtained was purified by silica gel column chromatography to produce 1.45 g of 3-(2-indanylacetyl)-L-thioproline ethyl ester as a colorless oil (yield: 57%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05028604 |
| Source dataset | uspto-grants-1991_07 |
| ORD ID | ord-a430a8c68ecf419ba0434ab8f081b75b |
| Source note | uspto-grants-1991_07 |