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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 233339Erstellt: 23. Oktober 2026

Hydrochloric Acid → methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)carbamate

https://huagongshe.com/de/reaction/233339

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktBromochloromethaneHCID 6333—
EduktChlorotrimethylsilaneHCID 6397—
Edukt(S)-Methyl 2-((methoxycarbonyl)amino)-3-phenylpropanoateHCID 10609905—
EduktHCID 178506865HCID 178506865—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelHexaneHCID 8058—
Produktmethyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)carbamateHCID 988153370%

Reaktionsschritte

15.4 ml of a 2.6 molar solution of hexyllithium in hexane were added dropwise at -80° C. to a solution of 9.50 g of methyl (S)-2-methoxycarbonylamino-3-phenyl-propionate in 60 ml of tetrahydrofuran. Subsequently, the mixture was treated with 5.60 ml of chlorotrimethylsilane. The resulting suspension was stirred and treated with 3.22 ml of bromochloromethane. Subsequently, 18.4 ml of hexyllithium solution were added. The solution was treated at -80° C. with 11 ml of 20% methanolic hydrochloric acid, warmed to 22° and diluted with 100 ml of water and 40 ml of tetrahydrofuran. The phases were separated and the organic phase was washed with saturated sodium chloride solution, dried and concentrated. The residue was recrystallized from ethyl acetate and hexane and the crystallizate was dried, there being obtained 7.20 g (70%) of pure methyl (S)-(1-benzyl-3-chloro-2-oxo-propyl)-carbamate, m.p. 122°-123° C. IR (KBr): 3336s (NH), 1737s and 1686s (C=O), 1535s (amide II).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05591885
Quelldatensatzuspto-grants-1997_01
ORD IDord-9bef9ffaabdf42c7983198d7d20b557d
Quellennotizuspto-grants-1997_01