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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1387469Generated: November 1, 2026

Ammonium Chloride → HCID 70235472, compound

https://huagongshe.com/reaction/1387469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant(+)-BenzylphenethylamineHCID 1268086—
ReactantHCID 54022061HCID 54022061—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 70235472HCID 70235472—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of N-benzyl-α-(R)-methylbenzylamine (0.82 g, 3.87 mmol) in THF (25 mL) at 0° C. was treated with n-BuLi (1.6 mL of a 2.5 M soln in hexanes). The resulting solution was stirred at 0° C. for 30 min and then cooled to −78° C. A solution of acrylate 20-5 (0.485 g, 1.76 mmol) in THF (5 mL) was added. After stirring for 15 min at −78° C., satd aq NH4Cl soln (5 mL) was added and the cold bath removed. The mixture was warmed to room temperature, and extracted with Et2O (2×40 mL). The combined organic extracts were washed with brine (30 mL), dried over MgSO4, filtered, and concentrated. The residue was purified by flash chromatography (40% ethyl acetate/hexanes) to give the β-aminoester 20-6 as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06268378B1
Source datasetuspto-grants-2001_07
ORD IDord-378a6ad6bfbe4272a122b5d54464ce47
Source noteuspto-grants-2001_07