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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1645306Generated: October 30, 2026

Dichloromethane → HCID 131728054, compound

https://huagongshe.com/reaction/1645306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 131728052HCID 131728052—
SolventPyridineHCID 1049—
ProductHCID 131728054HCID 131728054—

Reaction Steps

The mesylation of hydroxyl groups proceeds readily under these conditions (Protective Groups in Organic Synthesis, 3rd edition, 1999, pp. 150-160 and references cited therein). Briefly, to a solution of Compound 17 in a 1:1 mixture of anhydrous dichloromethane and anhydrous pyridine is added methanesulfonyl chloride (1.2 eq.). After stirring at room temperature for several hours, this mixture is quenched with methanol, concentrated, diluted with dichloromethane, washed with aqueous NaHCO3 and brine, dried over anhydrous Na2SO4, filtered and evaporated. Purification by silica gel chromatography will yield Compound 18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08124745B2
Source datasetuspto-grants-2012_02
ORD IDord-43fb00634f1b402781c832a7cd806011
Source noteuspto-grants-2012_02