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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759459Generated: October 31, 2026

Water → HCID 13046224, compound

https://huagongshe.com/reaction/1759459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetaminophenHCID 1983—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 13046223HCID 13046223—
SolventDimethylformamideHCID 6228—
ProductHCID 13046224HCID 1304622457.9%

Reaction Steps

A solution of 1.0 g (E)-4-bromo-1,1-diethoxy-2-methyl-2-butene in 10 ml of sieve dried dimethyl formamide is treated with 0.7 g of p-acetylaminophenol and 0.64 g anhydrous potassium carbonate. The suspension is stirred under nitrogen for four days and the mixture is then poured into 100 ml water and the hazy solution extracted with two 100 ml portions of benzene. The benzene extract is washed with water and dried with sodium sulfate. The benzene extract is concentrated and vacuum dried to give 0.75 g of (E)-4-(4-acetylaminophenoxy)-1,1-diethoxy-2-methyl-2-butene which is dissolved in about 5 to 10 ml acetone and treated with about 1 ml water and a spatula of p-toluenesulfonic acid monohydrate. The resulting solution is agitated occasionally for 30 minutes and the solution is evaporated at room temperature giving a solid, ethylether insoluble residue. The residue is dissolved in about 150 ml methylene chloride and washed twice with water. The residue is dried with sodium sulfate and concentration gave 0.45 g of a solid. The material is filtered in about 50 ml of hot carbon tetrachloride-benzene then boiled down to about 10 ml. The product is filtered and washed with room temperature carbon tetrachloride giving 0.2 g white solid, m.p. 127°-30° C. Elemental Analysis. Calculated for C13H15NO3 : C,66.94; H,6.48; N,6.00. Found: C,66.64; H,6.29; N,5.75.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04340765
Source datasetuspto-grants-1982_07
ORD IDord-c08c9e28248545938b619e1646502d19
Source noteuspto-grants-1982_07