HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 372822Generated: October 30, 2026
2-Chloroethyl vinyl ether → HCID 53704608, compound
https://huagongshe.com/reaction/372822
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroethyl vinyl ether | HCID 8074 | — |
| Reactant | 4-Phenoxyphenol | HCID 13254 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 53704608 | HCID 53704608 | — |
Reaction Steps
64 g of freshly distilled 2-chloroethyl-vinyl ether is placed into a flask; one drop of concentrated hydrochloric acid is added, and thereupon an addition is made in portions at room temperature, with stirring, of 93 g of 4-phenoxy-phenol (duration of addition about 1 hour). During the addition of 4-phenoxy-phenol, the temperature rises to about 32°- 34° C, with the 4-phenoxy-phenol completely dissolving. After two further hours' stirring, the reaction mixture is diluted with 300 ml of diethyl ether; the ether solution is washed three times with 10% potassium hydroxide solution and three times with saturated sodium chloride solution. The ether solution is subsequently dried over sodium sulphate, and the ether and the readily volatile constituents (traces of 2-chloroethyl-vinyl ether) are completely removed in vacuo. There is obtained 1-(2-chloroethoxy)-1-[(4-phenoxy)-phenoxy]-ethane in the form of colorless oil having a refractive index of nD20 = 1.5516 (yield 98%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04092365 |
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| Source dataset | uspto-grants-1978_05 |
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| ORD ID | ord-4bada0933290425db5dc75d93656184c |
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| Source note | uspto-grants-1978_05 |
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