HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 459719Generated: October 30, 2026
Trimethylsilyl isocyanate → HCID 21930997, compound
https://huagongshe.com/reaction/459719
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyl isocyanate | HCID 70696 | — |
| Reactant | tert-Butyl [2-(piperidin-3-yl)ethyl]carbamate | HCID 4362805 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21930997 | HCID 21930997 | 70.3% |
Reaction Steps
3-(2-tert-Butoxycarbonylaminoethyl)piperidine (500 mg, 2.19 mmoles) was dissolved in anhydrous dichloromethane (10 mL) and trimethylsilylisocyanate (2.96 mL, 21.9 mmoles) was added. The mixture was stirred under argon at 25° C. for 3.35 h. The mixture was diluted with dichloromethane and washed with saturated aqueous sodium bicarbonate. The organic layer was dried (MgSO4), filtered, evaporated to dryness and chromatographed on a silica gel column (15×5 cm) using 5% (10% conc. ammonium hydroxide in methanol)-dichloromethane as the eluant to give 3-(2-tert-butoxycarbonylaminoethyl)piperidine-1-carboxamide (417.7 mg, 70%): FABMS: m/z 272.0 (MH+); HRFABMS: m/z 272.1979 (MH+). Calcd. for C13H26O3: m/z 272.1974; δH (CDCl3) 1.16 (1H, m, CH2), 1–30–1.60 (5H, m, CH/CH2), 1.46 (9H, s, —COOC(CH3)3), 1.68 (1H, m, CH2), 1.84 (1H, m, CH2), 2.54 (1H, dd, CH2), 2.73 (1H, m, CH2), 3.08 (1H, m, CH2), 3.42 (1H, m, CH2), 4.02 (1H, m, CH2), 4.10 (1H, m, CH2), 4.84 (1H, m, NH) and 4.96 ppm (2H, bm, CONH2); δC (CDCl3) CH3: 28.5, 28.5, 28.5; CH2: 25.2, 31.7, 34.9, 37.3, 44.6, 50.3; CH: 32.9; C: 79.5, 156.4, 158.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07196078B2 |
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| Source dataset | uspto-grants-2007_03 |
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| ORD ID | ord-e3b1da06732f4f059c10b897a86f53d5 |
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| Source note | uspto-grants-2007_03 |
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