HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1042497Generated: October 31, 2026
Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester → HCID 66855506, compound
https://huagongshe.com/reaction/1042497
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester | HCID 17453 | — |
| Reactant | Aluminium lithium hydride | HCID 21226445 | — |
| Reactant | HCID 86649969 | HCID 86649969 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 66855506 | HCID 66855506 | 57.1% |
Reaction Steps
To a solution of N-methoxy-N-methyl-4-fluoro-2-ethylamino-benzamide (0.23 g, 1.02 mmol) in THF (4 mL) was added dropwise LiAlH4 (1 M in THF, 0.51 mL) at −45° C. The mixture was stirred for 40 minutes at −35° C. and then quenched by adding saturated aqueous KHSO4 solution. The mixture was diluted with EtOAc, washed with 3 N HCl, and brine, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was reacted with methyl (triphenylphosphoranylidene)acetate (375 mg, 1.12 mmol) in toluene (4 mL) overnight at 100° C. The mixture was washed with water, dried over anhydrous magnesium sulfate, filtered, and concentrated under reduced pressure to give the title compound (0.13 g, 57%) after purification by column chromatography (EtOAc:hexane=1:10).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08557872B2 |
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| Source dataset | uspto-grants-2013_10 |
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| ORD ID | ord-8081816f93614328935c335c3dbe4f8f |
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| Source note | uspto-grants-2013_10 |
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