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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297664Generated: October 30, 2026

Thionyl Chloride → HCID 86588179, compound

https://huagongshe.com/reaction/2297664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
ReactantHCID 14374715HCID 14374715—
SolventChloroformHCID 6212—
ProductHCID 86588179HCID 86588179113.6%

Reaction Conditions

Temperature20 °C

Reaction Steps

Thionyl chloride (4.3 ml) was added to a stirred solution of (3aS,4S,6R,6aR)-6-(6-chloro-purin-9-yl)-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxole4-carboxylic acid (10.0 g), in chloroform (100 ml). The mixture was heated at reflux temperature under nitrogen for 60 min. After cooling to 20° C. the solvent was removed in vacuo and the residue azeotroped with toluene (2×50 ml). A suspension of the residue in chloroform (50 ml) was added dropwise at an equal rate with a solution of 1-amino-2-propanol (2.3 ml) and diisopropylethylamine (5.1 ml) in chloroform (50 ml) over 10 min to chloroform (50 ml) at 0° C. The mixture was stirred at 20° C. for 18 hours. Phosphate buffer (pH 6.5, 100 ml) was added and the phases separated. The aqueous phase was extracted with chloroform (50 ml). The combined chloroform layers were dried with sodium sulphate and the solvent removed in vacuo to give the title compound as a white foam (6.63 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06492348B1
Source datasetuspto-grants-2002_12
ORD IDord-6c5e77d06a4d4ae59f2d51366062dfc0
Source noteuspto-grants-2002_12