HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 27605Generated: November 3, 2026
Chloride → beta-Dimethylaminoethyl 3-chloro-4-benzyloxyphenylacetate hydrochloride
https://huagongshe.com/reaction/27605
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | 2-(Dimethylamino)ethanol | HCID 7902 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Benzofenac | HCID 91676 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | beta-Dimethylaminoethyl 3-chloro-4-benzyloxyphenylacetate hydrochloride | HCID 23343310 | 131.1% |
Reaction Steps
6.15 grams of 3-chloro-4-benzyloxyphenylacetic acid was converted into the corresponding chloride by treatment with 15 ml of thionyl chloride in 50 ml of benzene. A solution comprising 1.85 grams of dimethylaminoethanol in 10 ml of benzene was slowly added at 20° C. to the chloride solution. The mixture was then permitted to stand for 2 hours at that temperature and then cooled to 5° C., so yielding a precipitate which was filtered and washed with benzene. Two crystallizations from ethylacetate-isopropyl alcohol (1:1) yielded 5.6 grams (68.4%) of β-dimethylaminoethyl 3-chloro-4-benzyloxyphenylacetate hydrochloride, m.p. 138°-140° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04221919 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-5a19c020631c4af9a138822f925c795b |
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| Source note | uspto-grants-1980_09 |
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