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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2100575Generated: October 27, 2026

Hexane → HCID 69055523, compound

https://huagongshe.com/reaction/2100575

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHexaneHCID 8058—
ReactantSodium hydrideHCID 24758—
ReactantBenzyl DimethylphosphonoacetateHCID 2773759—
ReactantHCID 86090086HCID 86090086—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69055523HCID 6905552397.6%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of hexane-washed sodium hydride (0.42 g of 60% suspension in mineral oil, 10.52 mmol) in 120 mL of THF at 0° C. was added benzyl 2-(dimethoxyphosphoryl)acetate (2.72 g, 10.52 mmol) dropwise in 10 mL of THF. The resulting mixture was stirred 5 min at 0° C. and then was allowed to warm to ambient temperature and stirred for 20 min. To this solution was added methyl 2-formyl-6-(trifluoromethyl)benzoate (2.22 g, 9.56 mmol) dropwise in 10 mL of THF. The resulting solution was stirred at ambient temperature for 1 h. The reaction mixture was quenched with 1N HCl (100 mL) and extracted with ethyl acetate. The organics were washed with sat'd aq NaHCO3 and brine, dried (MgSO4), filtered through a pad of silica gel and concentrated in vacuo to afford 3.4 g (97%) of the title compound which was sufficiently pure to be used without purification. 1H NMR (CDCl3): δ 7.79 (d, 1H, J=7.9 Hz), 7.72-7.67 (m, 2H), 7.55 (t, 1H, J=7.9 Hz), 7.38-7.30 (m, 5H), 6.47 (d, 1H, J=15.8 Hz), 5.23 (s, 2H), 3.94 (s, 3H). LRMS (ESI): 387.17 (M+H+Na)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07572805B2
Source datasetuspto-grants-2009_08
ORD IDord-944e7639aaad40a98363f692d256c5f8
Source noteuspto-grants-2009_08