HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Iodohexane → 5-(Hexyloxy)-2-methyl-1H-indole-3-acetic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Iodohexane | HCID 12527 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | O-Desmethyl-N-deschlorobenzoyl Indomethacin | HCID 11310252 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 5-(Hexyloxy)-2-methyl-1H-indole-3-acetic acid | HCID 19935757 | 62% |
Reaction Steps
To a solution of 5-hydroxy-2-methyl-1H-indole-3-acetic acid (7.17 g, 35.0 mmol) in methanol (40 mL) is added sodium methoxide (70 mmol). The solution is evaporated, dimethylformamide (40 mL) is added followed by hexyl iodide (35.0 mmol). After 2 days the solvent is removed and the residue is partitioned between ethyl acetate and pH=4 buffer. The organic layer is separated, dried over MgSO4 and evaporated to 8.6 g of a brown solid. Recrystallization from ethanol/water affords 6.23 g (62%) of white crystals, m.p. 65°-67° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05420289 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-2918c717de254b449985b0c368a94450 |
| Source note | uspto-grants-1995_05 |