HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1099368Generated: October 30, 2026
Hydrochloric Acid → 4-Hydroxy-2,3-dihydro-1H-indene-5-carbaldehyde
https://huagongshe.com/reaction/1099368
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Hydroxyindan | HCID 74233 | — |
| Reactant | Magnesium Chloride | HCID 5360315 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Hydroxy-2,3-dihydro-1H-indene-5-carbaldehyde | HCID 86643103 | 86% |
Reaction Steps
To a stirred suspension Magnesium chloride (71.0 gm, 0.745 mole) and Para-formaldehyde (33.6 gm, 1.12 mole) in Tetrahydrofuran (200 ml), Triethylamine (104 ml, 0.745 mole) was added at room temperature and stirred for 30 minutes. To the reaction mixture; the solution of Indan-4-ol (50 gm, 0.373) in Tetrahydrofuran (100 ml) was added at room temperature and heated to 70-75° C. for 6 hours. To the reaction mixture, 2N Hydrochloric acid (600 ml) was added and extracted with Ethylacetate (2×500 ml). The Ethylacetate layer was washed with water (300 ml), dried over Sodium sulphate and further it was distilled under vacuum to give viscous oil (52.0 gm) which becomes solid upon keeping.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143424B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-d93df2d7064e4f0594359a8cbb79fd26 |
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| Source note | uspto-grants-2012_03 |
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