HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → HCID 54490614, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 3,5-Dimethyl-4-nitrobenzaldehyde | HCID 12654144 | — |
| Reactant | Butyllithium | HCID 178418339 | — |
| Product | HCID 54490614 | HCID 54490614 | — |
Reaction Steps
To a stirred suspension of 3-(hydroxypropyl)triphenylphosphonium bromide (10.5 g) in dry THF (100 ml) at 0°, under nitrogen was added n-butyllithium (1.8 M in hexane, 30 ml). The stirring was continued at 0° for 30 min then a solution of 3,5-dimethyl-4-nitrobenzaldehyde (4.5 g) in dry THF (50 ml) was added over 10 min. The mixture was stirred at -10° for 1 h and at 0° for 1 h, saturated ammonium chloride (50 ml) was added and the mixture was extracted with EA (3×50 ml) the organic extracts were washed with water, brine, dried, concentrated and purified by [FCS] eluting with cyclohexane/EA 4:1 to give the title compound (1.05 g). T.l.c. (cyclohexane/EA 4:1) Rf 0.08.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04990505 |
| Source dataset | uspto-grants-1991_02 |
| ORD ID | ord-81f08d64500e452aa122c9d066a8c9f6 |
| Source note | uspto-grants-1991_02 |