HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2083498Generated: October 31, 2026
Hydrochloric Acid → [(3-Phenylacryloyl)oxy]acetic acid
https://huagongshe.com/reaction/2083498
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Glycolic Acid | HCID 757 | — |
| Reactant | 3-Phenylprop-2-enoyl chloride | HCID 66023 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | [(3-Phenylacryloyl)oxy]acetic acid | HCID 54392103 | 25.2% |
Reaction Steps
To a solution of glycolic acid (15.2 g.) in pyridine (100ml.) was added cinnamoyl chloride (33.4 g.) with stirring under cooling. The reaction mixture was stirred at room temperature for 5 hours and concentrated under reduced pressure at 50° to 60° C. The residue was adjusted to pH 1 with concentrated hydrochloric acid and extracted with ether. The extract was washed with water and a sodium chloride aqueous solution, in turn and concentrated under reduced pressure to give colorless crystals (45 g.). These crystals were dissolved in a sodium bicarbonate aqueous solution and adjusted to pH 3 to 3.5 with aqueous hydrochloric acid and extracted with ether. The extract was treated with a conventional manner to give crude product (16.5 g.). The product was recrystallized from benzene to give a product of 2-cinnamoyloxyacetic acid (10.4 g.), m.p. 116° to 121° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04085277 |
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| Source dataset | uspto-grants-1978_04 |
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| ORD ID | ord-db22d889831f441683a80cf5b3f31816 |
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| Source note | uspto-grants-1978_04 |
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