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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365003Generated: October 30, 2026

1-Methoxymethylcyclopropylsulfonylamine tert-butylcarbamate → 1-(Methoxymethyl)cyclopropane-1-sulfonamide

https://huagongshe.com/reaction/1365003

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Methoxymethylcyclopropylsulfonylamine tert-butylcarbamateHCID 66752382—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
Product1-(Methoxymethyl)cyclopropane-1-sulfonamideHCID 22499277—

Reaction Steps

A solution of 1-methoxymethylcyclopropylsulfonylamine tert-butylcarbamate (1.14 g, 4.30 mmol) was dissolved in a solution of 50% TFA/dichloromethane (30 mL) and was stirred at room temperature for 16 hours. The solvent was removed in vacuo and the residue chromatographed over 80 g of SiO2 (eluting with 0% to 60% ethyl acetate/hexanes to 1-methoxymethylcyclopropylsulfonamide as a white solid (0.55 g, 77% overall over two steps): 1H NMR (CDCl3) δ 0.95 (m, 2H), 1.44 (m, 2H), 3.36 (s, 3H), 3.65 (s, 2H), 4.85 (s, 2H); 13C NMR (CDCl3) δ 11.17, 40.87, 59.23, 74.80; LRMS m/z 183 (M++NH4).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888464B2
Source datasetuspto-grants-2011_02
ORD IDord-4417e0894bb24718afb71b5b8a9f2ebb
Source noteuspto-grants-2011_02