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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2359273Generated: November 2, 2026

Methanesulfonyl chloride → HCID 56592714, compound

https://huagongshe.com/reaction/2359273

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 58046306HCID 58046306—
SolventTetrahydrofuranHCID 8028—
ProductHCID 56592714HCID 56592714—

Reaction Steps

To a solution of 4-(3,4-dichlorobenzyl)-3-methoxybenzamide (Preparation 155, 155 mg, 0.50 mmol) in anyhydrous THF (5 mL) was added 1M LiHMDS (1.25 mL, 1.25 mmol) via syringe. The mixture was stirred for 20 minutes before adding mesyl chloride (0.116 mL, 1.50 mmol) and then stirred for 18 hours at room temperature. The reaction was quenched with the addition of 2M HCl (20 mL), and the aqueous was extracted with EtOAc (3×20 mL). The combined organics were concentrated in vacuo and the residue was purified by silica gel column chromatography eluting with a gradient of 25% EtOAc in heptane to 100% EtOAc. The title compound was obtained as a white solid (40 mg, 21%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08685977B2
Source datasetuspto-grants-2014_04
ORD IDord-ca2bb36889ba49ee987d5d94f2afe278
Source noteuspto-grants-2014_04