HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1097258Generated: October 30, 2026
2-(Benzyloxy) ethanol → ethyl 5-fluoro-1-(2-benzyloxyethyl)-1H-indole-2-carboxylate
https://huagongshe.com/reaction/1097258
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-(Benzyloxy) ethanol | HCID 12141 | — |
| Reactant | ethyl 5-fluoro-1H-indole-2-carboxylate | HCID 2727899 | — |
| Reactant | Cyanomethylenetrimethylphosphorane | HCID 11094579 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | ethyl 5-fluoro-1-(2-benzyloxyethyl)-1H-indole-2-carboxylate | HCID 66811343 | 88.1% |
Reaction Steps
94 μl (0.657 mmol) of 2-benzyloxyethanol and 50.4 mg (0.438 mmol) of (cyanomethylene)trimethylphosphorane (Tet. Lett., 1996, 37, 2459-2462) are added to a solution of 68 mg (0.329 mmol) of ethyl 5-fluoro-1H-indole-2-carboxylate in 2 ml of toluene, stirred at 20° C. The reaction mixture is heated at 110° C. for 12 hours and then concentrated under reduced pressure, taken up in 20 ml of ethyl ether, filtered over a celite buffer and concentrated under reduced pressure. The residue obtained is purified by preparative HPLC, elution being carried out with a mixture of water, acetonitrile and trifluoroacetic acid. 99 mg of a yellow oil are thus isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143248B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-0f405a7e438d4facac24934ed65fcd91 |
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| Source note | uspto-grants-2012_03 |
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