HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Triphenylphosphoranylidene)acetone → HCID 67086773, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Triphenylphosphoranylidene)acetone | HCID 15038 | — |
| Reactant | 3-Thiophenecarboxaldehyde, 2,4,5-trichloro- | HCID 173786 | — |
| Catalyst | Lithium Bromide | HCID 82050 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 67086773 | HCID 67086773 | 91.3% |
Reaction Steps
To a stirred solution of 2,4,5-trichloro-thiophene-3-carbaldehyde (10.3 g; 48 mmol) and lithium bromide (0.10 g; 1.2 mmol) in acetonitrile (100 mL) at 15° C. under nitrogen was added acetylmethylene-triphenylphosphorane (15.6 g; 49 mmol). The reaction mixture was stirred for 3 hours at ambient temperature then poured in water (200 ml) and extracted with dichloromethane (3×70 ml). Combined organic layers were dried over anhydrous sodium sulphate. The solvent was removed in vacuo and the residue was purified by chromatography over silica gel (eluant: cyclohexane/ethyl acetate 90:10) to afford 11.2 g (91% of theory) of (E)-4-(2,4,5-trichloro-thiophen-3-yl)-but-3-en-2-one as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08357635B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-411bd0ef44fe492bb8df82547a1ba29f |
| Source note | uspto-grants-2013_01 |