HuagongsheHuagongshe Chemistry Print Report · For research reference only
(Diethylamino)sulfur trifluoride → HCID 15060970, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (Diethylamino)sulfur trifluoride | HCID 123472 | — |
| Reactant | HCID 88527862 | HCID 88527862 | — |
| Product | HCID 15060970 | HCID 15060970 | — |
Reaction Steps
N.m.r. in solvent C: 2.9 (s, 3H), 3.5 (t, 2H), 4.5 t, 2H , 6.65 s, 1H , 7.3 (s, 15H). 6. N.m.r. in solvent C: 3 0 (s, 3H), 3.5-3.7 (m, 4H), 4.3 (m, 2H), 4.7 (m, 2H), 5.1 (d, 1H), 5.9 (d, 1H) 6.8 (s, 1H), 7.4 (s, 15H). 7. N.m.r. in solvent A: 3.4 (s, 2H), 3.9 (d, 1H), 4.4 (d, 1H), 4.8 (s, 2H , 4.9 (d, 1H), 5.7 (d, 1H), 6.8 (s, 1H), 7.2 (s, 15H). 8. The starting material may be prepared as follows. Reaction of ethyl 2-(2-tritylaminothiazol-4-yl)-2-[(Z)-2-hydroxyethoxyimino]acetate with diethylamino sulphur trifluoride and hydrolysis of the resulting ester gave 2-(2-tritylaminothiazol-4-yl)-2[(Z)-2-fluoroethoxyimino]acetic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05049558 |
| Source dataset | uspto-grants-1991_09 |
| ORD ID | ord-c8d9fab651194b2483126baf119821dc |
| Source note | uspto-grants-1991_09 |