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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880019Generated: November 1, 2026

Methanol → Tert-butyl (1-(3,4-dichlorophenylsulfonyl)pyrrolidin-2-yl)methylcarbamate

https://huagongshe.com/reaction/880019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBenzenesulfonyl chloride, 3,4-dichloro-HCID 7383—
ReactantTriethylamineHCID 8471—
ReactantPyrrolidin-2-ylmethyl-carbamic acid tert-butyl esterHCID 21834643—
SolventDichloromethaneHCID 6344—
ProductTert-butyl (1-(3,4-dichlorophenylsulfonyl)pyrrolidin-2-yl)methylcarbamateHCID 8673007898%

Reaction Steps

To a solution of 3,4-dichlorobenzene-1-sulfonyl chloride (490 mg, 2.00 mmol) was added tert-butyl pyrrolidin-2-ylmethylcarbamate (400 mg, 2.00 mmol), followed by triethylamine (0.278 mL, 2.00 mmol). The reaction was stirred at rt overnight. The reaction mixture was diluted with DCM and washed with 1N HCl, H2O and brine, dried over Na2SO4 and decanted. The solvent was evaporated under reduced pressure and the crude product was purified on a 24 g silica gel cartridge using 0 to 100% EtOAc in hexane for 15 min, then 0 to 20% MeOH in DCM for 15 min to provide Intermediate 2A (800 mg, 1.95 mmol, 98% yield) as a white solid. HPLC/MS (Method D) RT=2.12 min, [M+1]+ 309.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993557B2
Source datasetuspto-grants-2015_03
ORD IDord-4611673fddb94d27bf6bb581fc4e0f46
Source noteuspto-grants-2015_03