HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1888077Generated: October 31, 2026
Ethanolamine → tert-Butyl 4-aminomethyl-4-fluoropiperidine-1-carboxylate
https://huagongshe.com/reaction/1888077
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | Tert-butyl 4-((1,3-dioxoisoindolin-2-yl)methyl)-4-fluoropiperidine-1-carboxylate | HCID 53415317 | — |
| Product | tert-Butyl 4-aminomethyl-4-fluoropiperidine-1-carboxylate | HCID 40152119 | — |
Reaction Steps
A mixture of 3-3 (11.0 g) and 25 mL ethanolamine was stirred at 60° C. for 1 h. The reaction was then allowed to cool to room temperature, poured into ice-water (100 mL), and extracted with CH2Cl2 (3×100 mL). The combined organic layers were washed with brine (150 mL), dried over MgSO4, filtered, and concentrated in vacuo, giving 5.82 g of crude 3-4 as a viscous amber oil. 1H NMR (CDCl3, 300 MHz): 3.94 (br, 2H), 3.08 (m, 2H), 1.85 (m, 2H), 1.51 (m, 4H), 1.44 (s, 9H); MS (Electrospray): m/z 218.2 (M−Me+H), 177.2 (M−t−Bu+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08501773B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-3aff64ee755c4a5faffbcb56488be7ee |
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| Source note | uspto-grants-2013_08 |
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