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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989473Generated: October 30, 2026

Methanol → 5'-O-tert-butyldiphenylsilyl-N6-benzoyl-2'-O-(formylmethyl)-adenosine

https://huagongshe.com/reaction/989473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant5'-O-tert-butyldiphenylsilyl-N6-benzoyl-2'-O-(2,3-dihydroxypropyl)-adenosineHCID 57291736—
SolventDichloromethaneHCID 6344—
Product5'-O-tert-butyldiphenylsilyl-N6-benzoyl-2'-O-(formylmethyl)-adenosineHCID 53664412105.2%

Reaction Steps

Compound 112 (5.59 g, 8.17 mmol) was dissolved in dry CH2Cl2 (40.42 mL). To this NaIO4 adsorbed on silica gel (Ref. J. Org. Chem. 1997, 62, 2622-2624) (16.34 g, 2 g/mmol) was added and stirred at ambient temperature for 30 minutes. Reaction monitored by TLC (5% MeOH in CH2Cl2). Reaction mixture was filtered and the filtrate washed thoroughly with CH2Cl2. Dichloromethane layer evaporated to get the aldehyde 113 (5.60 g) that was used in the next step without purification. Rf 0.3 (5% MeOH in CH2Cl2)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06639062B2
Source datasetuspto-grants-2003_10
ORD IDord-dad27ca9455a49a8959303b56f59d403
Source noteuspto-grants-2003_10