HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 512602Generated: October 27, 2026
Bromoform → 2-(4-Isopropoxyphenyl)-2-methoxyacetic acid
https://huagongshe.com/reaction/512602
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromoform | HCID 5558 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 4-Isopropoxybenzaldehyde | HCID 250077 | — |
| Reactant | Potassium hydroxide methanol | HCID 23689386 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2-(4-Isopropoxyphenyl)-2-methoxyacetic acid | HCID 58432042 | — |
Reaction Steps
An oven-dried flask was charged with 4-isopropoxybenzaldehyde (4.9 g, 29.9 mmol), anhydrous methanol (30 mL) and anhydrous dioxane (30 mL) then fitted with an addition funnel. The addition funnel was charged with a solution of KOH (8.4 g, 149.5 mmol) in anhydrous methanol (30 mL) and an aliquot (˜2 mL) was added to the reaction mixture. Bromoform (3.4 mL, 38.8 mmol) was added to the reaction mixture then the remaining KOH/MeOH solution was added dropwise over 10 minutes. After stirring for 18 hours, the mixture was concentrated in vacuo. The residue was diluted with water and the pH was adjusted to ˜2 using concentrated HCl then extracted with EtOAc. The combined organics were dried over Na2SO4 and filtered. Concentration of the filtrate in vacuo gave 2-(4-isopropoxyphenyl)-2-methoxyacetic acid as a light yellow solid (6.8 g) which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09102643B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-45a2465395e64d92b8c2514d44a98544 |
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| Source note | uspto-grants-2015_08 |
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