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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 431822Erstellt: 25. Oktober 2026

Sodium hydride → (2S,4R)-2-(2,4,5-trifluoro-benzyloxymethyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/431822

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
EduktAmmonium ChlorideHCID 25517—
Edukt2,4,5-Trifluorobenzyl BromideHCID 2777057—
Edukt(2S,4R)-2-hydroxymethyl-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 11271474—
LösungsmittelDimethylformamideHCID 6228—
Produkt(2S,4R)-2-(2,4,5-trifluoro-benzyloxymethyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 1178688746,4%

Reaktionsschritte

A solution of 15.5 g (32.59 mmol) (2S,4R)-2-Hydroxymethyl-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl ester and 24.7 g (109.77 mmol) 2,4,5-trifluoro-benzylbromide in 700 ml DMF at 0° C. was treated with 2.28 g (52.14 mmol) of 55% NaH in 4 portions and warmed up to RT during 7 h. The reaction was cooled to 0° C. and treated with 500 ml aqueous saturated NH4Cl solution, extracted with EtOAc (3×). The organic phase was washed with 10% NaCl dried over Na2SO4 and evaporated. Flash column chromatography on silica gel with hexane/EtOAc (9:1 to 8.5:1.5) gave 9.37 g (46%) of (2S,4R)-2-(2,4,5-Trifluoro-benzyloxymethyl)-4-tritylsulfanyl-pyrrolidine-1-carboxylic acid tert-butyl ester, MS: 620 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06660738B2
Quelldatensatzuspto-grants-2003_12
ORD IDord-39065d201d054f71a56e22b30c240a31
Quellennotizuspto-grants-2003_12