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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606192Generated: October 30, 2026

Potassium Hydroxide → HCID 57078752, compound

https://huagongshe.com/reaction/1606192

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant2-ThiophenemethanolHCID 69467—
ReactantHCID 11424363HCID 11424363—
SolventDiethyl EtherHCID 3283—
ProductHCID 57078752HCID 57078752—

Reaction Steps

Diethyl ether. To a suspension of 1.32 g. (0.01 mole) of cloromethylthiophene [obtained by the method of F. F. BLICKE, J.A.C.S. 64, 477 (1942)] and 1.2 g. (0.02 mole) of powdered potassium hydroxide in 10 ml. of ether there is added a solution of 3.5 g. (0.03 mole) of thenyl alcohol in 10 ml. of ether. The reaction mixture is stirred for 1 hour at room temperature, then refluxed for 30 minutes and finally allowed to stand over night. After filtration the ethereal solution is concentrated and the residue fractionally distilled. There is obtained 0.22 g. (10%) of dithenyl ether having a b.p. of 99°C./0.01 mm. Hg. and a m.p. of 36.5°. 1c. Furfuryl thenyl ether is obtained by the same method as used for preparing compound (1) b., but using furfuryl alcohol instead of thenyl alcohol. The product thus obtained had a b.p. of 50°C./0.01 mm. Hg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03952024
Source datasetuspto-grants-1976_04
ORD IDord-4e31d65b2a2545829d181fd0d31d70b5
Source noteuspto-grants-1976_04