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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 969711Generated: November 1, 2026

Dichlorodimethylsilane → 2,6-Dichloropurine

https://huagongshe.com/reaction/969711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichlorodimethylsilaneHCID 6398—
ReactantIsoamyl NitriteHCID 8053—
ReactantHCID 10149094HCID 10149094—
CatalystBenzyl triethylammonium chlorideHCID 66133—
Solvent1,2-DichlorobenzeneHCID 7239—
Product2,6-DichloropurineHCID 532441272.6%

Reaction Conditions

Temperature27.5 °C

Reaction Steps

9-Acetyl-2-amino-6-chloropurine (2.50 g, 11.8 mmol), dichlorodimethylsilane (4.57 g, 35.4 mmol), benzyltriethylammonium chloride (0.16 g, 0.70 mmol) and isoamyl nitrite (2.07 g, 17.7 mmol) were added to o-dichlorobenzene (10 ml), and the mixture was heated to 25-30° C. and stirred for 8 hr. After the completion of the reaction, the mixture was filtrated. The obtained crystals were diluted with water (4.0 ml), and the reaction mixture was added dropwise to 2M aqueous sodium hydroxide solution (20 ml) and partitioned. The aqueous layer was adjusted to pH 4-5 with 35% hydrochloric acid. After aging under ice-cooling for 1 hr, the mixture was filtrated, and the obtained crystals were dried under reduced pressure at 80° C. to give 2,6-dichloropurine as a white powder (1.62 g, yield 72.6%). The properties of the obtained compound were the same as in Example 1(2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07307167B2
Source datasetuspto-grants-2007_12
ORD IDord-575825576c19492d8de4acc092c51aeb
Source noteuspto-grants-2007_12