HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170830Generated: November 1, 2026
Di-tert-butyl dicarbonate → HCID 10968084, compound
https://huagongshe.com/reaction/1170830
Participants
| Role | Name | HCID | Charge |
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| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | HCID 1514115 | HCID 1514115 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 10968084 | HCID 10968084 | — |
Reaction Steps
To a solution of (S)-piperidine-2-carboxylic acid tert-butyl ester (M. Egbertson and S. J. Danishefsky, J. Org. Chem., 1989, 54, 1, 11-12) (5.78 g, 31.2 mmol) in CH3CN (30 mL) at 0° C. was added DMAP (763 mg, 6.2 mmol) followed by BOC2O (10.22 g, 46.8 mmol). The reaction mixture was allowed to warm to room temperature and stirred for 20 h. The solvents were evaporated under reduced pressure and the residue was purified by flash chromatography (10% ethyl acetate in hexane). The title compound was obtained as a colourless oil which crystallized upon standing (8.33 g, 94%): 1H NMR (400 MHz, CDCl3) δ 1.21-1.32 (2H, m), 1.47-1.48 (18H, 2 s), 1.59-1.72 (3H, m), 2.18 (1H, m), 2.85-3.00 (1H, m), 3.89-4.01 (1H, 2 d, J=11.9 Hz), 4.47-4.58 (1H, 2br s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07829561B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-490c9d2228e744118308122b3ada78b2 |
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| Source note | uspto-grants-2010_11 |
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