HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1606192Generated: October 30, 2026
Potassium Hydroxide → HCID 57078752, compound
https://huagongshe.com/reaction/1606192
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Thiophenemethanol | HCID 69467 | — |
| Reactant | HCID 11424363 | HCID 11424363 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 57078752 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03952024 |
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| Source dataset | uspto-grants-1976_04 |
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| ORD ID | ord-4e31d65b2a2545829d181fd0d31d70b5 |
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| Source note | uspto-grants-1976_04 |
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