HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186899Generated: November 3, 2026
Trimethylsilyl isocyanate → HCID 21930997, compound
https://huagongshe.com/reaction/1186899
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), 184 (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 | US08673924B2 |
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| Source dataset | uspto-grants-2014_03 |
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| ORD ID | ord-2a1d98ec548d4df4997840fa2394697a |
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| Source note | uspto-grants-2014_03 |
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