HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 963745Generated: October 31, 2026
2-Chloroethanol → HCID 22447375, compound
https://huagongshe.com/reaction/963745
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroethanol | HCID 34 | — |
| Reactant | 2-Methylbut-3-enoic acid | HCID 143088 | — |
| Catalyst | 2-Amino-3,4-dimethylpyridine | HCID 11007884 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | HCID 22447375 | HCID 22447375 | 85.1% |
Reaction Steps
45.1 g (0.45 mol) of 2-methyl-3-butenoic acid, 45.33 g (0.56 mol) of 2-chloroethanol and 4.1 g (34 mmol) of dimethyl-aminopyridine were placed in 450 ml of diethyl ether under argon. 102.2 g (0.495 mol) of N,N-dicyclohexylcarbodiimide were added thereto in 5 portions at 0° C. within 30 minutes, the mixture was stirred at room temperature for a further 2 hours and the separated urea was filtered off. The filtrate was washed in succession with 200 ml of 0.5N aqueous hydrochloric acid, 100 ml of saturated sodium bicarbonate solution and 100 ml of saturated sodium chloride solution. The organic solution was dried over anhydrous 2 0 sodium sulphate and, after concentration, the product was distilled on a Vigreux column (20 cm) at 80°-81° C./10 mbar. This gave 62.3 g (83% yield) of 2-methyl-but-3-enoic acid 2-chloroethyl ester as a colourless oil with a content of 97.5% according to GC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05763651 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-3fcc5bddd6dd4eb9bd80614f5bca6c34 |
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| Source note | uspto-grants-1998_06 |
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