HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methoxymethylcyclopropylsulfonylamine tert-butylcarbamate → 1-(Methoxymethyl)cyclopropane-1-sulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methoxymethylcyclopropylsulfonylamine tert-butylcarbamate | HCID 66752382 | — |
| Solvent | Trifluoroacetic acid methylene chloride | HCID 21863450 | — |
| Product | 1-(Methoxymethyl)cyclopropane-1-sulfonamide | HCID 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 111.7, 40.87, 59.23, 74.80; LRMS m/z 183 (M++NH4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07964560B2 |
| Source dataset | uspto-grants-2011_06 |
| ORD ID | ord-614b6a5182e94b2d920e92f1b5c8fb21 |
| Source note | uspto-grants-2011_06 |