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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1815703Generated: November 1, 2026

1-Methylcyclopropane-1-sulfonamide → 1-Propylcyclopropane-1-sulfonamide

https://huagongshe.com/reaction/1815703

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methylcyclopropane-1-sulfonamideHCID 21889814—
ReactantHCID 69266674HCID 69266674—
Product1-Propylcyclopropane-1-sulfonamideHCID 2249936080%

Reaction Steps

Step 29b) This compound was made from Compound 29a in 80% yield (25.15 g) from N-tert-butyl-(1-propyl) cyclopropylsulfonamide (42.2 g, 193 mmol) according to the procedure of Steps 3Id (Example 2) described in the synthesis of 1-methylcyclopropylsulfonamide. The compound was recrystallized from EtOAc/hexanes as a white solid: 1H NMR CHLOROFORM-D) δ ppm 0.85 (m, 2H), 0.94 (t, J=7.32 Hz, 3H), 1.36 (m, 2H), 1.47 (m, 2H), 1.87 (m, 2H), 4.42 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06878722B2
Source datasetuspto-grants-2005_04
ORD IDord-9fef5e6b0bab4d60a1e597d88cf8eac1
Source noteuspto-grants-2005_04