HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166450Generated: October 28, 2026
Dicyclohexylcarbodiimide → HCID 86584774, compound
https://huagongshe.com/reaction/1166450
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | (S)-2-((tert)-Butoxycarbonyl)amino)butanoic acid | HCID 2755934 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86584774 | HCID 86584774 | 88% |
Reaction Steps
BOC-homoalanine (Podlech, J.; Seebach, D. (1995) Liebigs Ann. 1217) (0.44 g, 2.17 mmol) was dissolved in 5 mL methylene chloride. HOSu (376.4 mg, 3.27 mmol) was added and the solution cooled to 0° C. After addition of DCC (587.8 mg, 2.85 mmol) the solution was stirred 1 hour at 0° C., warmed to room temperature and stirred for an additional 2 hours. A stream of methylamine was bubbled through the suspension for 10 minutes, and stirring was continued overnight. The white precipitate was filtered off by suction filtration and the filtrate concentrated to give a pale yellow solid that was purified by chromatography (silica gel, CHCl3/MeOH 19:1) to yield 0.41 g (1.90 mmol, 88%) Of BOC-homoalanine methylamide (18) as a white solid. 1H-NMR (300 MHz, CDCl3) δ 6.11 (b, NH), 5.23 (b, NH), 3.92 (m, 1H), 2.75 (d, J=4.8 Hz, 3H), 2.35 (m, 2H), 1.39 (s, 9H), 1.17 (d, J=6.6 Hz, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06613876B1 |
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| Source dataset | uspto-grants-2003_09 |
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| ORD ID | ord-a1e00ca10ad54b588b23d5203394d289 |
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| Source note | uspto-grants-2003_09 |
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