HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874789Generated: October 26, 2026
Triphenylphosphine → methyl 5-{[(2,2-dimethyl-1,3-dioxan-5-yl)methyl]oxy}-1H-indole-2-carboxylate
https://huagongshe.com/reaction/1874789
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | (2,2-Dimethyl-1,3-dioxan-5-yl)methanol | HCID 3584869 | — |
| Reactant | methyl 5-hydroxy-1H-indole-2-carboxylate | HCID 21904362 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | methyl 5-{[(2,2-dimethyl-1,3-dioxan-5-yl)methyl]oxy}-1H-indole-2-carboxylate | HCID 59451360 | 93.9% |
Reaction Steps
Methyl 5-Hydroxy-1H-indole-2-carboxylate (0.10 g, 0.5 mmol), triphenylphosphine (0.28 g, 1.0 mmol), diethyl azodicarboxylate (0.18 g, 1.0 mmol) and (2,2-dimethyl-1,3-dioxan-5-yl)methanol (0.15 g, 1.0 mmol) were dissolved in CH2Cl2 (5 mL) and the mixture was stirred overnight. The solvent was evaporated. Purification was accomplished by Reverse-Phase HPLC (water/acetonitrile with 0.1% TFA). The desired fractions were neutralized with saturated NaHCO3 and extracted with EtOAc. The organic extracts were combined dried over Na2SO4, filtered and evaporated to afford the title compound (0.15 g, 90%) as a tan solid. 1H NMR (400 MHz, DMSO-d6): δ ppm 11.74 (br. s., 1H), 7.29 (d, 1H), 7.09 (d, 1H), 7.01 (d, 1H), 6.88 (dd, 1H), 3.92-4.01 (m, 4H), 3.81 (s, 3H), 3.72 (dd, 2H), 1.97-2.08 (m, 1H), 1.31 (s, 3H), 1.28 (s, 3H). MS: m/z 342.2 (M+23).
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-bdf74f0af1ba40a5a3fb1d0cdcebe4b8 |
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| Source note | uspto-grants-2012_11 |
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