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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 362607Generated: October 30, 2026

Methanol → HCID 136344604, compound

https://huagongshe.com/reaction/362607

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantStearoyl chlorideHCID 8212—
ReactantSodium BicarbonateHCID 516892—
Reactant(R)-9-[2-Hydroxymethyl 4-(t-butyldiphenylsilyloxy)butyl]guanineHCID 136344530—
SolventPyridineHCID 1049—
SolventDichloromethaneHCID 6344—
ProductHCID 136344604HCID 136344604—

Reaction Steps

(R)-9-[2-Hydroxymethyl 4-(t-butyldiphenylsilyloxy)butyl]guanine (2.31 g, 5 mmole) was coevaporated with dry pyridine twice and dissolved in pyridine (20 ml). To the solution was slowly added dropwise stearoyl chloride (1.86 ml, 5.5 mmole, technical grade) in dichloromethane (2 ml) at -5° C. The reaction was kept at the same temperature for 1 hr and then at 5° C. for 2 hr. The reaction was monitored by TLC. Additional stearoyl chloride (0.29 ml) at -5° C. was added due to incompletion of reaction. After 30 min at 5° C., methanol (3 ml) was added and the reaction mixture stirred for 20 min. It was then poured into aqueous sodium hydrogen carbonate solution, and extracted with dichloromethane. The organic phase was dried and the product purified by silica ge column chromatography with stepwise increasing MeOH, eluting with 3.5% MeOH in CH2Cl2 (Yield 2.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05869493
Source datasetuspto-grants-1999_02
ORD IDord-881e2746e05c497590605bf75e0d0356
Source noteuspto-grants-1999_02