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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1904993Generated: October 31, 2026

Methanesulfonyl chloride → HCID 13923448, compound

https://huagongshe.com/reaction/1904993

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 13062021HCID 13062021—
SolventPyridineHCID 1049—
ProductHCID 13923448HCID 1392344890%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-ethyl-5'-O-trityl-2'-deoxyuridine (7.5 g, 15 mmole) in dry pyridine (50 ml), methanesulfonyl chloride (4.0 g, 35 mmole) is added while cooling in an ice-water bath. The mixture is stirred for one hour at around 0° C. and followed by allowing the temperature to rise to room temperature. At this point, tlc indicates no remaining starting materials. The mixture is then poured into an ice-water mixture (1.5 liters) while stirring, the water is decanted, and the product is washed with cold water several times, dissolved in chloroform and dried (over MgSO4). Finally, the solvent is evacuated in vacuo to obtain a syrup (7.6 g, 90%). This material is sufficiently pure to carry out the next reaction without further purification. However, an analytical sample can be obtained by column chromatography or tlc using chloroform as an eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04841039
Source datasetuspto-grants-1989_06
ORD IDord-39d2e7b9b9c04e98909c937e23e95f06
Source noteuspto-grants-1989_06