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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339156Generated: October 25, 2026

N-tert-butyl-3-chloropropane-1-sulfonamide → N-tert-Butylcyclopropanesulfonamide

https://huagongshe.com/reaction/339156

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-tert-butyl-3-chloropropane-1-sulfonamideHCID 11701296—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductN-tert-ButylcyclopropanesulfonamideHCID 2249930156.4%

Reaction Steps

To a solution of N-tert-butyl-(3-chloro)propylsulfonamide (2.14 g, 10.0 mmol) in THF (100 mL) was added n-BuLi (2.5 M in hexane, 8.0 mL, 20.0 mmol) at −78° C. The reaction mixture was allowed to warm up to room temperature over period of 1 h. The volatiles were removed in vacuo. The residue was partitioned between EtOAC and water (200 mL, 200 mL). The separated organic phase was washed with brine, dried over Na2SO4, filtered and concentrated in vacuo. The residue was recrystallized from hexane to yield the desired product as a white solid (1.0 g, 56%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889871B2
Source datasetuspto-grants-2014_11
ORD IDord-5f0473953fab46668f705a9dd975081f
Source noteuspto-grants-2014_11