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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2199102Generated: October 29, 2026

Dimethylamine → 2,4-Xylenol, 6-chloro-alpha(sup 4)-(dimethylamino)-

https://huagongshe.com/reaction/2199102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylamineHCID 674—
ReactantFormaldehydeHCID 712—
Reactant2-Chloro-6-methylphenolHCID 6898—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product2,4-Xylenol, 6-chloro-alpha(sup 4)-(dimethylamino)-HCID 306812566%

Reaction Steps

A solution of 2-chloro-6-methyl phenol (5.0 g, 0.035 mol) in ethanol (25 mL) at room temperature was treated with dimethyl amine (3.95 mL of a 40% solution of dimethylamine in water, 0.035 mol) followed by formaldehyde (2.85 mL of a 37% solution of formaldehyde in water, 0.035 mol). The reaction was heated to reflux for 24 h. At this time, the reaction mixture was cooled to room temperature and concentrated under vacuum. The resulting oil was diluted with water (200 mL) and acidified to pH=2 by addition of a 1N aqueous hydrochloric acid solution. The water layer was extracted with ethyl acetate (300 mL). The ethyl acetate layer was discarded. The water layer was made basic to pH=10 by the addition of a 1N aqueous sodium hydroxide solution and was extracted with ethyl acetate (2×350 mL). The organics were washed with a saturated aqueous sodium chloride solution, dried with magnesium sulfate, filtered and concentrated under vacuum. The resulting oil was dried under high vacuum overnight to afford 2-chloro-4-dimethylaminomethyl-6-methyl-phenol (2b) (4.62 g, 66%) as an off-white solid; EI(+)-HRMS m/z calcd for C10H14ClNO (M+) 199.0764, found 199.0767. Molecular Weight=199.6822; Exact Mass=199.0764

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE046024E1
Source datasetuspto-grants-2016_06
ORD IDord-e8a99a53e78d43f6b6903dc1f494f7c6
Source noteuspto-grants-2016_06