HuagongsheHuagongshe Chemistry Print Report · For research reference only
Indole → ethyl trans-2-((1H-indol-1-yl)methyl)cyclopropanecarboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Indole | HCID 798 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 2-(((methylsulfonyl)oxy)methyl)cyclopropanecarboxylate | HCID 57184993 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl trans-2-((1H-indol-1-yl)methyl)cyclopropanecarboxylate | HCID 67290699 | 54% |
Reaction Steps
To a suspension of sodium hydride (60%, 55 mg, 1.4 mmol) in DMF (5 mL) was added indole (135 mg, 1.2 mmol). After stirring at room temperature for 10 min, ethyl 2-(((methylsulfonyl)oxy)methyl)cyclopropanecarboxylate (307 mg, 1.4 mmol) was added. After stirring at room temperature for 6 h, the mixture was poured into water, and the aqueous layer was extracted with EtOAc twice. The combined organic layer was dried over sodium sulfate and concentrated in vacuo. The residue was purified by column chromatography on silica gel eluting with hexane/ethyl acetate (10:1-5:1) to give 153 mg (54%) of the title compound as a pale brown oil;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09101616B2 |
| Source dataset | uspto-grants-2015_08 |
| ORD ID | ord-0f75e6b3148947f98c16685a91637156 |
| Source note | uspto-grants-2015_08 |