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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1655766Generated: November 2, 2026

Ammonium Chloride → HCID 57014599, compound

https://huagongshe.com/reaction/1655766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactanttert-butyl N-[(2S)-4-methyl-1-oxopentan-2-yl]carbamateHCID 104275—
ReactantMagnesiumHCID 5462224—
ReactantHCID 53991717HCID 53991717—
SolventDiethyl EtherHCID 3283—
Solvent1,2-DibromoethaneHCID 7839—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57014599HCID 5701459942.6%

Reaction Steps

A solution of 40.9 g (0.18 mol) of (S)-(-)-2-phenyl-3-methylbromobutane in 110 ml of tetrahydrofuran and 0.5 ml of 1,2-dibromoethane was slowly added dropwise to a suspension of 6.6 g of magnesium in 25 ml of ether. The temperature rose to 50°. Thereafter, the reaction mixture was stirred at 50° for a further 2 hours and then cooled to -50°. Then, a solution of 13 g (0.06 mol) of N-t-butoxycarbonyl-L-leucinal in 40 ml of tetrahydrofuran was added slowly. After 16 hours at room temperature, the reaction mixture was treated with 200 ml of a 20% ammonium chloride solution. The organic phase was dried over magnesium sulfate and the solvent was evaporated under reduced pressure. The residue (24.3 g) was chromatographed on silica gel with a 4:1 mixture of hexane and ether, to obtain 9.3 g of t-butyl [(1S,2S,4S)-2-hydroxy-1-isobutyl-5 -methyl-4-phenylhexyl]carbamate which has a melting point of 95°-96° after crystallization from hexane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05250517
Source datasetuspto-grants-1993_10
ORD IDord-dd9052d8ba0d4b97827a8e4b562cc087
Source noteuspto-grants-1993_10