HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 964871Generated: October 30, 2026
Sodium Hydroxide → 3-Allyloxy-benzoic acid
https://huagongshe.com/reaction/964871
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Sodium Bisulfate | HCID 516919 | — |
| Reactant | HCID 11321926 | HCID 11321926 | — |
| Solvent | Methanol--water (1/1) | HCID 22242641 | — |
| Product | 3-Allyloxy-benzoic acid | HCID 6483884 | 97.8% |
Reaction Steps
A solution of 917 mg (4.2 mmol) of 3-(2-propenyloxy)benzoic acid, 2-propenyl ester in 9 mL of methanol/water (3:2) at room temperature is treated with 0.53 mL (5.25 mmol) of 10M sodium hydroxide solution. The solution is allowed to stir for one hour then acidified with 5 mL of 10% sodium bisulfate solution and extracted with 25 mL of ethyl acetate. The organic layer is washed with saturated sodium chloride solution, dried over magnesium sulfate, and concentrated in vacuo to give 732 mg (97%) of 3-(2-propenyloxy)benzoic acid as a white powder. The product is utilized in the next reaction without further purification; m.p. 78°-79°; the 1H NMR (300 MHz, CDCl3) is consistent with the desired product; IR (KBr) 3000, 1690, 1620, 1590 cm-1 ; MS (CI low res) m/e 179 (M+H), 161, 135; Analysis calculated for C10H10O3 : C, 67.41; H, 5.66; found: C, 67.37; H, 5.59.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05773001 |
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| Source dataset | uspto-grants-1998_06 |
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| ORD ID | ord-fd62647bd8d34f6c8788a2813a470c81 |
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| Source note | uspto-grants-1998_06 |
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