HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → (S)-6-Benzyloxy-2,5,7,8-tetramethylchroman-2-ethanol methanesulfonate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 11067787 | HCID 11067787 | — |
| Reactant | HCID 70588933 | HCID 70588933 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | (S)-6-Benzyloxy-2,5,7,8-tetramethylchroman-2-ethanol methanesulfonate | HCID 54156209 | — |
Reaction Steps
A solution of 0.5 g. (1.47 mmoles) of (S)-(-)-6-benzyloxy-2,5,7,8-tetramethylchroman-2-ethanol and 0.25 ml. (0.37 g.; 3.2 mmoles) of methanesulfonyl chloride in 5 ml. of anhydrous pyridine was kept at 0° C. for 45 hours then poured into 100 ml. of ice-water and the resulting mixture was stirred for 15 minutes. The mixture was then extracted three times with ether and the combined ether extracts were washed with cold 1 N aqueous HCl followed by water and saturated brine. After drying and filtration, the ether extracts were concentrated in vacuo giving 0.587 g. (95.6%) of (S)-6-benzyloxy-2,5,7,8-tetramethylchroman-2-ethanol methane as a colorless solid, m.p. 81°-83° C.; [α]25D-0.36° (c 0.82, C6H6).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04151205 |
| Source dataset | uspto-grants-1979_04 |
| ORD ID | ord-f83c7d66660141078d1628d50ff5589c |
| Source note | uspto-grants-1979_04 |