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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 458295Generated: October 25, 2026

Benzyl Alcohol → 6-(Phenylmethoxy)-9H-purin-2-amine

https://huagongshe.com/reaction/458295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantNitrogenHCID 947—
ReactantSodium hydrideHCID 24758—
Reactant2-Amino-6-chloropurineHCID 5360349—
SolventTolueneHCID 1140—
Product6-(Phenylmethoxy)-9H-purin-2-amineHCID 4578—

Reaction Conditions

Temperature115 °C

Reaction Steps

60% Sodium hydride in mineral oil (2.36 g, 0.059 moles) was charged to a 500 mL 3-neck flask equipped with magnetic stirring, temperature probe, condenser, and N2 inlet. Toluene (250 mL) was added. Benzyl alcohol (50 mL) was added dropwise over 30 minutes. After addition of benzyl alcohol, the reaction was stirred 10 minutes. Then 6-chloro-2-aminopurine (5.00 g, 0.029 moles) was added and the reaction mixture was heated to reflux (115° C.) for 4.5 hours. The reaction mixture was filtered hot through a coarse glass fritted funnel and 11.65 g of wet off-white solids were obtained. The wet solids were triturated with CH2Cl2 (100 mL) and water (100 mL). After 10 minutes of stirring the solids had dissolved. The aqueous layer was separated and the pH was lowered to 9 over 3 minutes with 6 M HCl. A white solid precipitate formed. The slurry was filtered, washed with water (50 mL), and dried (in vacuo at 50° C.) to a constant weight to provide the desired product as off-white crystals (5.15 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07189849B2
Source datasetuspto-grants-2007_03
ORD IDord-b128acacab3c4a0381b11082d87f1ad6
Source noteuspto-grants-2007_03