HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1788895Generated: November 2, 2026
1-Ethyl-4-hydroxy-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic Acid Methyl Ester → HCID 13911142, compound
https://huagongshe.com/reaction/1788895
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethyl-4-hydroxy-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic Acid Methyl Ester | HCID 14064723 | — |
| Reactant | HCID 178419663 | HCID 178419663 | — |
| Catalyst | Titanium Tetrachloride | HCID 24193 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 13911142 | HCID 13911142 | 51.5% |
Reaction Steps
To a solution of 1-ethyl-4-hydroxy-1,3,4,9-tetrahydropyrano[3,4-b]indole-1-acetic acid methyl ester (1 g, 3.6 mmol) in 60 mL of dry methylene chloride at -78° C. under nitrogen was added TiCl4 in one portion and then after ~10 minutes, a solution of benzyl magnesium bromide in ether was added in one portion and the reaction mixture was allowed to stir at -78° C. for ~30 minutes. The reaction was quenched with methanol (3 mL) at -78° C. and then poured into water (10 mL). The two layers were separated and the aqueous layer was then extracted with methylene chloride (2×100 mL), dried over magnesium sulfate and concentrated in vacuo. The crude product was passed through a pad of silica gel, eluting with 10% EtOAc in hexane to give 0.67 g (51.5%) of the product as an oil, which had isomer ratio of 75:25 by HPLC.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04686213 |
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| Source dataset | uspto-grants-1987_08 |
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| ORD ID | ord-3c249d2ea45e4d7eb9c39839b84aa498 |
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| Source note | uspto-grants-1987_08 |
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