HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1371551Generated: November 3, 2026
Methyl 3-(3-(N-Boc-piperidin-4-yl)-propoxy)-phenylacetate → 3-(3-(N-Boc-piperidin-4-yl)-propoxy)-phenylacetic acid
https://huagongshe.com/reaction/1371551
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl 3-(3-(N-Boc-piperidin-4-yl)-propoxy)-phenylacetate | HCID 21071299 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 3-(3-(N-Boc-piperidin-4-yl)-propoxy)-phenylacetic acid | HCID 21071295 | — |
Reaction Steps
Methyl 3-(3-(N-Boc-piperidin-4-yl)-propoxy)-phenylacetate (0.5 g, 1.3 mmol) was dissolved in methanol, and 2N NaoH (3 mL) added. The reaction was stirred at 60° C. for 2 h, then the solution was adjusted to pH 6.5, the product was extracted into ethyl acetate and the organic phase was dried by MgSO4. Removal of solvent revealed 3-(3-(N-Boc-piperidin-4-yl)-propoxy)-phenylacetic acid (0.30 g). 1H NMR (500 MHz, CDCl3) δ 1.02 (m, 2H), 1.25 (m, 2H), 1.55 (m, 2H), 1.65 (m, 2H), 2.57 (m, 2H), 3.33 (m, 1H), 3.75 (s, 2H), 3.95 (m, 2H), 6.63 (m, 3H), 6.98 (m, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07157476B2 |
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| Source dataset | uspto-grants-2007_01 |
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| ORD ID | ord-025a2aba906b405ab46770df3fe7a8a2 |
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| Source note | uspto-grants-2007_01 |
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