HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → HCID 22168556, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Potassium bisulfate | HCID 516920 | — |
| Reactant | HCID 22168635 | HCID 22168635 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 22168556 | HCID 22168556 | 59% |
Reaction Steps
Allyl 3-methylthio-5-nitrobenzoate (1.12 g, 4.4 mM) was dissolved in methanol (30 ml), and cooled to 2°. A solution of “potassium peroxymonopersulfate” (2 KHSO5.KHSO4.K2SO4, 8.13 g, 13.2 mM) in water (25 ml) was added slowly, and stirring continued for 4 hours. The mixture was diluted with water (60 ml) and extracted with ethyl acetate (3×100 ml). The combined organic extracts were washed with water, brine, and dried over Na2SO4. Crude product was purified by chromatography on silica using a gradient of petrol/ethyl acetate (3:1 to 2:1) to give allyl 3-methylsulphonyl-5-nitrobenzoate (0.74 g, 59%). Nmr (DMSO-d6): δ 3.44 (s, 3H); 4.94 (dt, 2H); 5.32-5.53 (m, 2H); 6.01-6.25 (m, 1H); 8.78 (t, 1H); 8.89 (t, 1H); 8.91 (t, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07041836B2 |
| Source dataset | uspto-grants-2006_05 |
| ORD ID | ord-27513ac11cf0426fb6ca4a773d496461 |
| Source note | uspto-grants-2006_05 |