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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714168Generated: October 30, 2026

3-Hydroxybenzaldehyde → HCID 242135, compound

https://huagongshe.com/reaction/714168

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-HydroxybenzaldehydeHCID 101—
ReactantAcetoneHCID 180—
ReactantHydrochloric AcidHCID 313—
ReactantSodium HydroxideHCID 14798—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 242135HCID 24213519%

Reaction Steps

3-Hydroxybenzaldehyde (1p, 2.07 g, 17.0) and acetone (19, 0.62 ml, 8.4 mmol) were combined in ethanol (15 ml) and stirred for 15 min at room temperature. A solution of sodium hydroxide (1.00 g, 25.0 mmol) and water (4 ml) was added and the solution stirred for 48 hr at room temperature. The resulting mixture was neutralized with hydrochloric acid (1 N), extracted with ethyl acetate, washed with saturated sodium chloride, dried over magnesium sulfate, filtered and evaporated to afford a solid. The crude solid was recrystallized from ethyl acetate to give 0.42 g (19%) of a brown solid: mp 190-195° C. [expected mp 198-200° C.]; 1H NMR: (DMSO) δ 6.83 (d, 2H, J=7.0 Hz), 7.22 (m, 8H), 7.68 (d, 2H, J=16.1 Hz), 9.63 (s, 2H); 13C NMR: (DMSO) δ 114.7, 117.5, 119.4, 125.4, 129.7, 135.8, 142.7, 157.5, 168.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187397B2
Source datasetuspto-grants-2015_11
ORD IDord-02233957f3574becb22b99963d86290a
Source noteuspto-grants-2015_11