HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2210051Generated: November 2, 2026
2-Methoxybenzaldehyde → 1-Hydroxy-7-methoxy-1,3-dihydrobenzo[c]furan
https://huagongshe.com/reaction/2210051
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methoxybenzaldehyde | HCID 8658 | — |
| Reactant | Acetic acid, 2-(triphenylphosphoranylidene)-, methyl ester | HCID 17453 | — |
| Reactant | 7-methoxy-3H-isobenzofuran-1-one | HCID 10986583 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-Hydroxy-7-methoxy-1,3-dihydrobenzo[c]furan | HCID 13613689 | — |
| Product | Methyl 2E-3-(2-hydroxymethyl-6-methoxyphenyl)acrylate | HCID 19598060 | — |
Reaction Steps
1-Hydroxy-7-methoxy-1,3-dihydrobenzo[c]furan (1.08 g), which was prepared with using 7-methoxyphthalide which was synthesized with using 2-methoxybenzaldehyde by the method described in Journal of Organic Chemistry, 1980, 45, 1835-1838, was dissolved in chloroform (20 ml). Methyl (triphenylphosphoranylidene)acetate (2.68 g) was added to the solution. The mixture was stirred for 40 min. at 50° C. A temperature of the reaction mixture was down to room temperature. The reaction solution was purified by column chromatography on silica gel (n-hexane:ethyl acetate=2:1) to give the title compound (1.25 g) having the following physical data.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05457122 |
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| Source dataset | uspto-grants-1995_10 |
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| ORD ID | ord-bf4ee21eb7b94f47ab3758936b7b45a2 |
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| Source note | uspto-grants-1995_10 |
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