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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465643Generated: October 30, 2026

3-Chloro-1,2-propanediol → HCID 58442471, compound

https://huagongshe.com/reaction/1465643

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-1,2-propanediolHCID 7290—
Reactant1-(4-Hydroxy-2,6-dimethylphenyl)ethanoneHCID 4057370—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
ProductHCID 58442471HCID 5844247157.4%

Reaction Conditions

Temperature140 °C

Reaction Steps

A pressure glass vessel charged with 1-(4-hydroxy-2,6-dimethylphenyl)ethanone (2.00 g, 12.2 mmol, 1.0 equiv) and 3-chloropropane-1,2-diol (1.02 mL, 12.2 mmol, 1.0 equiv) in 50% aqueous NaOH solution (20.0 mL) was heated at 140° C. for 16 h. The mixture was diluted with H2O (20 mL) and extracted with EtOAc. The organic layer was collected, dried over MgSO4(s), and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (30% EtOAc in hexanes as eluant) to provide 1-(4-(2,3-dihydroxypropoxy)-2,6-dimethylphenyl)ethanone (1.66 g, 7.0 mmol) as yellow oil in 57% yield: 1H NMR (CDCl3, 500 MHz) δ o 6.57 (s, 2 H), 4.10-4.11 (m, 1 H), 4.08-4.09 (m, 2 H), 4.01-4.02 (m, 1 H), 3.74-3.75 (m, 1 H), 2.58-2.59 (s, 1 H), 2.45 (s, 3 H), 2.23 (s, 6 H), 2.05-2.10 (s, 1 H); ESI-MS: m/z 239.9 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999983B2
Source datasetuspto-grants-2015_04
ORD IDord-08d7add772ad4de299cb37527b8fbf64
Source noteuspto-grants-2015_04