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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815706Generated: October 29, 2026

Chlorosuccinimide → HCID 86591859, compound

https://huagongshe.com/reaction/1815706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosuccinimideHCID 31398—
ReactantCyclopropylsulfonylamine tert-butylcarbamateHCID 68821921—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86591859HCID 8659185979.8%

Reaction Conditions

Temperature-78 °C

Reaction Steps

step 3.8a) To a solution of cyclopropylsulfonylamine tert-butyl carbamate (1.0 g, 4.52 mmol) dissolved in THF (10 mL) cooled to −78° C., was added n-BuLi (6.4 mL, 10.2 mmol, 1.6 M in hexane) and the reaction mixture was stirred for 1 h. To this solution was added a THF (10 mL) solution of NCS (0.86 g, 6.34 mmol). After stirred for 5 min, the bath was changed to ice bath and the mixture was stirred for 3 h at the temperature. The reaction mixture was diluted with ice water, the pH was adjusted to <4. The aqueous mixtire was extracted with EtOAc. The combined extracts were dried (MgSO4), concentrated and purified by flash chromatography over SiO2 using EtOAc/hexanes (0% to 60%) as the eluent to afford 0.98 g (67%) of 1-chloro-cyclopropanesulfonamide-tert-butylcarbamate as a white solid: 1H NMR (CDCl3) δ ppm 1.51 (m, II H), 2.01 (m, 2H), 7.60 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878722B2
Source datasetuspto-grants-2005_04
ORD IDord-907fd717db194e92bdd5e1c7404a39f6
Source noteuspto-grants-2005_04