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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1035852Generated: October 26, 2026

Hydrochloric Acid → HCID 67034854, compound

https://huagongshe.com/reaction/1035852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,2,4-TrimethoxybenzeneHCID 67284—
Reactant6-Bromohexanoyl chlorideHCID 89848—
ReactantAluminum(III) ChlorideHCID 6451240—
SolventDichloromethaneHCID 6344—
ProductHCID 67034854HCID 6703485499%

Reaction Conditions

Temperature-10 °C

Reaction Steps

6 ml (40 mmol) of 1,2,4-trimethoxybenzene are introduced into 80 ml of dry CH2Cl2 and the mixture is cooled to −10° C. with stirring. 6-Bromohexanoyl chloride (6.2 ml, 40 mmol) dissolved in 20 ml of CH2Cl2 is then added dropwise. AlCl3 (5.6 g, 42 mmol) is progressively introduced in small portions into the reaction mixture. The reaction is maintained with stirring for 8 h with a return to ambient temperature. The reaction mixture is then poured onto ice (200 ml) and acidified to pH 1 using HCl. The mixture is stirred until it returns to ambient temperature, 1 h. After evaporation of the CH2Cl2, the mixture is extracted with AcOEt, and the organic phases are separated, dried over MgSO4, filtered and evaporated. The residue is subjected to flash chromatography over SiO2 with a gradient of pure heptane to heptane-AcOEt 50-50. The pure fractions are evaporated to obtain 13.6 g (yield=99%) of crystals. TLC SiO2 (heptane-ACOEt 70-30) Rf=0.5; 1H NMR (CDCl3): 7.41 (s, 1H), 6.50 (s, 1H), 3.95 (s, 3H), 3.91 (s, 3H), 3.87 (s, 3H), 3.43 (t, 2H, J=6.76 Hz), 2.98 (t, 2H, J=6.32 Hz), 1.91 (m, 2H), 1.71 (m, 2H), 1.51 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546402B2
Source datasetuspto-grants-2013_10
ORD IDord-d4f51fb9fd954286a380b0216e1f134f
Source noteuspto-grants-2013_10