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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 611461Erstellt: 24. Oktober 2026

Sodium hydride → HCID 54170183, Verbindung

https://huagongshe.com/de/reaction/611461

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium hydrideHCID 24758—
Edukt1-(Bromomethyl)-4-(1,1-dimethylethyl)benzeneHCID 87836—
EduktAdenosine, N-benzoyl-5'-O-(bis(4-methoxyphenyl)phenylmethyl)-2'-deoxy-HCID 2724489—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 54170183HCID 5417018328,5%

Reaktionsschritte

To N6 -benzoyl-5'-O-(4,4'-dimethoxytrityl)-2'-deoxyadenosine (658 mg, 1.0 mmole) was added DMF (anhydrous, 10 ml) and evaporated to dryness. This was repeated. Fresh DMF (10 ml) was added under an Argon atmosphere. Sodium hydride (44 mg, 60% in oil, 1.1 mmole) was added and the mixture was stirred for 0.5 hour at room temperature. 4-(tert-butyl)benzyl bromide (272 mg, 1.2 mmole) was added dropwise and stirred at room temperature overnight. The solvent was removed under vacuum, and the residue was partitioned between ethyl acetate and water (20 ml each). The organic phase was washed with water (3 times, 20 ml), dried over anhydrous magnesium sulfate, filtered and evaporated to dryness. The crude product was purified by column chromatography on silica gel (100 g), using methylene chloride:methanol:triethylamine 96.5:3:0.5 to yield N -benzoyl-N -(p-tert-butylbenzyl)-5'-O-(4,4'-dimethoxytrityl)-2'-deoxyadenosine, (229 mg, 28.5%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06001611
Quelldatensatzuspto-grants-1999_12
ORD IDord-c768af7a0d224101ae34deeda17aa3c6
Quellennotizuspto-grants-1999_12