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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1972634Generated: November 1, 2026

Ammonium Chloride → HCID 66582880, compound

https://huagongshe.com/reaction/1972634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 66582819HCID 66582819—
ReactantHCID 178419101HCID 178419101—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66582880HCID 6658288098.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

A 150-mL round-bottomed flask was charged with 4-benzyl 1-tert-butyl 2-oxo-1,4-piperazinedicarboxylate (1.41 g, 4.22 mmol) and THF (5 mL). 1-Propynylmagnesium bromide (0.5 M in THF, 20.0 mL, 10.0 mmol, Sigma-Aldrich, St. Louis, Mo.) was added at 0° C. slowly. The mixture was stirred at 0° C. for 2 h. Saturated aqueous NH4Cl (40 mL) was added and the aqueous phase was extracted with EtOAc (200 mL, then 2×100 mL). The combined organic phases were dried over sodium sulfate, filtered and concentrated in vacuo. The crude product was purified by column chromatography (50 g of silica, 0 to 50% EtOAc in hexanes) to afford benzyl (2-((tert-butoxycarbonyl)amino)ethyl)(2-oxo-3-pentyn-1-yl)carbamate (1.55 g) as a clear oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431563B2
Source datasetuspto-grants-2013_04
ORD IDord-92750f86e4084d6d8fa52ee9747e5c05
Source noteuspto-grants-2013_04