HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874948Generated: November 1, 2026
Methanol → 5-(2-hydroxyethoxy)-1H-indole-2-carboxylic acid
https://huagongshe.com/reaction/1874948
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Lithium Hydroxide | HCID 3939 | — |
| Reactant | HCID 86761647 | HCID 86761647 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-(2-hydroxyethoxy)-1H-indole-2-carboxylic acid | HCID 18455622 | 16% |
| Product | HCID 68485440 | HCID 68485440 | 7% |
Reaction Steps
A methanol solution of 1-(1,1-dimethylethyl)2-ethyl 5-[(2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}ethyl)oxy]-1H-indole-1,2-dicarboxylate (0.200 g, 0.431 mmol) was treated with 1 N LiOH (4 mL). A precipitate formed and THF was added to redissolve the material. The reaction was heated to 70° C. until the starting material was consumed, partitioned between EtOAc and water and the layers separated. The basic aqueous layer was acidified with conc. HCl and extracted with EtOAc. Purification was accomplished by silica gel column chromatography (0-100% EtOAc/hexanes, striped with MeOH) to afford the title compound (0.015 g, 16%) and 5-[(2-{[(1,1-dimethylethyl)(dimethyl)silyl]oxy}ethyl)oxy]-1H-indole-2-carboxylic acid (0.0114 g, 7%) 1H NMR (400 MHz, Acetone-d6) δ ppm 10.73 (br. s., 1H), 7.43 (d, 1H), 7.15 (d, 1H), 7.10 (d, 1H), 6.96 (dd, 1H), 4.07 (t, 2H), 3.88 (t, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304419B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-45ac2a52a60e41f3bce3c4b49340bdf9 |
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| Source note | uspto-grants-2012_11 |
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