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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166450Generated: October 28, 2026

Dicyclohexylcarbodiimide → HCID 86584774, compound

https://huagongshe.com/reaction/1166450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
Reactant(S)-2-((tert)-Butoxycarbonyl)amino)butanoic acidHCID 2755934—
SolventDichloromethaneHCID 6344—
ProductHCID 86584774HCID 8658477488%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613876B1
Source datasetuspto-grants-2003_09
ORD IDord-a1e00ca10ad54b588b23d5203394d289
Source noteuspto-grants-2003_09