HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2291912Generated: November 1, 2026
Chloroacetyl chloride → 3-alpha-Chloroacetyl-2-[(o-hydroxyphenoxy)methyl]thiazolidine
https://huagongshe.com/reaction/2291912
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Phenol, 2-(2-thiazolidinylmethoxy)- | HCID 3025464 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 3-alpha-Chloroacetyl-2-[(o-hydroxyphenoxy)methyl]thiazolidine | HCID 10085477 | — |
Reaction Steps
Chloroacetylchloride (2.5 ml) is added to a stirred solution of 2-[(o-hydroxyphenoxy)methyl]thiazolidine (6 g) in 1,2-dichloroethane (80 ml) and triethilamine (4.3 ml) cooled at -30° C. After the usual work-up 3-α-chloroacetyl-2-[(o-hydroxyphenoxy)methyl]thiazolidine (5.7 g, from Et2O, m.p. 89°-91° C.) is obtained. A stirred solution of the latter compound in 1,2-dichloroethane (50 ml) is heated with solid potassium thioacetate (4 g). After 2 hours, the mixture is washed with water to give, after the usual work-up, 3-acetylthio-acetyl-2-[(o-hydroxyphenoxy)methyl]thiazolidine (6.4 g, from EtOH) m.p. 97°-99° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04798898 |
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| Source dataset | uspto-grants-1989_01 |
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| ORD ID | ord-da687f3dbb5447a78a7c42df039f8d2d |
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| Source note | uspto-grants-1989_01 |
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