HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338449Generated: October 29, 2026
3-Pyridinemethanol → HCID 86698781, compound
https://huagongshe.com/reaction/338449
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Pyridinemethanol | HCID 7510 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | HCID 86698779 | HCID 86698779 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86698781 | HCID 86698781 | — |
Reaction Steps
A mixture of 1-tert-butyl 3-methyl 6-chloro-5-(4-hydroxyphenyl)-1H-indole-1,3-dicarboxylate (30 mg, 0.075 mmol), polymer supported triphenylphosphine (50 mg, 0.15 mmol), anhydrous tetrahydrofuran (1.0 mL), pyridin-3-ylmethanol (0.015 mL, 0.15 mmol), and bis(2-methoxyethyl)-diazene-1,2-dicarboxylate) (35 mg, 0.15 mmol) was sealed in a vial and stirred vigorously at 70° C. for 18 hours. The cooled reaction mixture was filtered through a pad of Celite, and the filter pad was washed with diethyl ether twice. The filtrate was concentrated in vacuo, and the residue partitioned between diethyl ether and water. The organic layer was separated and washed sequentially with water and then brine. The ether layer was concentrated in vacuo and to give the title compound, which was used directly in the next step. MS (ES+) 493 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889730B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-593f8f1cb4de4590ac5adf50c3d500b5 |
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| Source note | uspto-grants-2014_11 |
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