HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Toluenesulfonyl chloride → ((5R)-2-oxo-1,3-oxazolidin-5-yl)methyl4-methylbenzenesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Toluenesulfonyl chloride | HCID 7397 | — |
| Reactant | (5R)-5-(hydroxymethyl)-1,3-oxazolidin-2-one | HCID 10236003 | — |
| Reactant | Sodium chloride dihydrate | HCID 23713072 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | ((5R)-2-oxo-1,3-oxazolidin-5-yl)methyl4-methylbenzenesulfonate | HCID 2793763 | — |
Reaction Steps
A solution of (5R)-5-(hydroxymethyl)-1,3-oxazolidin-2-one (10.0 g), prepared as described in Tetrahedron: Asymmetry 1995, 6, 1181-1190, in pyridine (60 mL) at −10° C. was treated with para-toluenesulfonyl chloride (21.2 g), stirred for 2 hours, poured into 1:1 brine/water (100 mL), and extracted with ethyl acetate. The extract was washed with 1:1 saturated sodium bicarbonate/water and 1:1 brine/water, and the washes were back extracted with ethyl acetate. The combined extracts was dried (MgSO4), filtered, and concentrated to provide the desired product. MS (ESI(+)) m/e 272 (M+H)+; 1H NMR (300 MHz, CDCl3) δ 7.80 (d, 2H), 7.39 (d, 2H), 4.80 (m, 1H), 4.18 (d, 2H), 3.70 (t, 1H), 3.50 (dd, 1H), 2.45 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06277868B1 |
| Source dataset | uspto-grants-2001_08 |
| ORD ID | ord-5c581483aa0943ae8a4be73ea380bc95 |
| Source note | uspto-grants-2001_08 |