HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401136Generated: October 29, 2026
Tributylphosphine → N-Boc-3-(2-piperidin-4-yl-ethoxy)-benzoic acid ethyl ester
https://huagongshe.com/reaction/1401136
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tributylphosphine | HCID 13831 | — |
| Reactant | Ethyl 3-hydroxybenzoate | HCID 24522 | — |
| Reactant | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| Reactant | 1-(tert-Butoxycarbonyl)-4-(2-hydroxyethyl)piperidine | HCID 854140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-Boc-3-(2-piperidin-4-yl-ethoxy)-benzoic acid ethyl ester | HCID 66930054 | 97.8% |
Reaction Steps
N-Boc-4-piperidine ethanol (15 g, 65 mmol) and ethyl 3-hydroxybenzoate (11 g, 65 mmol) were dissolved in dry THF (750 ml) under N2. To this was added tri-n-butylphosphin (24 ml, 98 mmol) and ADDP (25 g, 98 mmol) resulting in a suspension, which was stirred overnight at 20° C. The mixture was concentrated in vacuo to ˜100 ml, filtered, and the filtrate was evaporated with silica gel. Flash chromatography (EtOAc/heptane 1:4) afforded 24 g of the title compound. LC-MS (m/z): 401 (M+23).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08907096B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-c55cce2106a445f8bc09ca0263e6649b |
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| Source note | uspto-grants-2014_12 |
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