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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1276545Generated: October 25, 2026

Benzaldehyde → Benzylidene Dihexanoate

https://huagongshe.com/reaction/1276545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantSulfuric AcidHCID 1118—
ReactantCarbon TetrachlorideHCID 5943—
ReactantHexanoic anhydrideHCID 74918—
ProductBenzylidene DihexanoateHCID 22116394—

Reaction Steps

Benzaldehyde (26.3 g, 0.25 mol) and hexanoic acid anhydride (53.3 g, 0.25 mol) were dissolved in carbontetrachloride (200 ml) under N2 -atrnosphere. Catalytic amounts of sulfuric acid was added and the reaction mixture stirred at room temperature for 1 hr. The reaction mixture was evaporated over night, the residue dissolved in hexane and the solution filtered through a bed of silica. The filtrate was purified on a silica column, eluting with hexane. The evaporated eluate was a colourless oil and the yield was 14.0 g, 18% of the theoretical. 1H- and 13C NMR (CDCl3) d (ppm) rel. to TMS: 7.72 (s, 1H, CH(OC5H11)2), 7.58-7.39 (m, 5H, Ar-H), 2.37 (double t, 4 H, COCH2), 1.64 (m, 4H, COCH2CH2), 1.30 (m, 4H,CH2CH2CH3) and 0.88 (t, 6H, CH3); 171.524 (C=O), 135.688, 129.523, 128.466 and 126.547 (Ar), 89.398 (CH(OC5H11)2), 33.965, 31.030, 24.235 and 22.179 (CH2) and 13.777 (CH3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06166074
Source datasetuspto-grants-2000_12
ORD IDord-0ac83dd932234a3e9b8cd9b5398f47aa
Source noteuspto-grants-2000_12