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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic acid, 2-(triphenylphosphoranylidene)-, methyl esterHCID 17453—
ReactantAluminium lithium hydrideHCID 21226445—
ReactantHCID 86649969HCID 86649969—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66855506HCID 6685550657.1%

Reaction Conditions

Temperature-35 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557872B2
Source datasetuspto-grants-2013_10
ORD IDord-8081816f93614328935c335c3dbe4f8f
Source noteuspto-grants-2013_10