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| | Methyl (5-hydroxy-2,3-dihydro-1H-inden-1-yl)acetate Basic information |
| Product Name: | Methyl (5-hydroxy-2,3-dihydro-1H-inden-1-yl)acetate | | Synonyms: | 2-(5-hydroxyindan-1-yl)acetate;Methyl 2-(5-hydroxyindan-1-yl)acetate;Methyl 2-(5-hydroxy-2,3-dihydro-1H-inden-1-yl)acetate;1H-Indene-1-acetic acid, 2,3-dihydro-5-hydroxy-, methyl ester;Methyl (5-hydroxy-2,3-dihydro-1H-inden-1-yl)acetate | | CAS: | 856169-08-9 | | MF: | C12H14O3 | | MW: | 206.24 | | EINECS: | | | Product Categories: | | | Mol File: | 856169-08-9.mol |  |
| | Methyl (5-hydroxy-2,3-dihydro-1H-inden-1-yl)acetate Chemical Properties |
| Boiling point | 339.0±35.0 °C(Predicted) | | density | 1.181±0.06 g/cm3(Predicted) | | storage temp. | Sealed in dry,Room Temperature | | pka | 10.25±0.40(Predicted) |
| | Methyl (5-hydroxy-2,3-dihydro-1H-inden-1-yl)acetate Usage And Synthesis |
| Synthesis | The general procedure for the synthesis of methyl 2-(5-hydroxy-1-indenyl)acetate from the compound (CAS: 1187199-58-1) is as follows:
1. a mixture of methyl 2-(5-(benzyloxy)-2,3-dihydroinden-1-ylidene)acetate (5.3, 3.44 g, 11.7 mmol) with Pd-C (1.38 g, 11.7 mmol) in methanol (35 mL) was stirred for 3 hours under hydrogen atmosphere.
2. Upon completion of the reaction, the mixture was filtered through silica gel to remove the Pd-C catalyst.
3. After the solvent was removed under pressure, the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane, 1:2) to afford the racemic product in 47% yield.
4. Separation of the racemic product using a chiral column (OD column, eluent: 4% isopropanol/hexane) afforded (R)-2-(5-hydroxy-2,3-dihydro-1H-inden-1-yl)methyl acetate (31.1, 0.324 g, retention time: 23.9 min, >99% ee) and (S)-2-(5-hydroxy-2,3-dihydro-1H-inden-1-yl)acetic acid (31.1, 0.324 g, retention time: 23.9 min, >99% ee). -yl)acetic acid methyl ester (31.2, 0.315 g, retention time: 30.4 min, >99% ee).
For the steps of Synthesis 5.4:
1. a mixture of methyl 2-(5-(benzyloxy)-2,3-dihydroinden-1-ylidene)acetate (5.3, 3.44 g, 11.7 mmol) with Pd-C (1.38 g, 11.7 mmol) in methanol (35 mL) was stirred for 3 hours under hydrogen atmosphere.
2. Upon completion of the reaction, the mixture was filtered through silica gel to remove the Pd-C catalyst.
3. After the solvent was removed under pressure, the residue was purified by silica gel column chromatography (eluent: ethyl acetate/hexane, 1:2) to afford the racemic product in 47% yield.
4. Separation of the racemic product using a chiral column (OD column, eluent: 4% isopropanol/hexane) gave 5.4 (>99% ee). | | References | [1] Patent: WO2009/111056, 2009, A1. Location in patent: Page/Page column 273; 318 |
| | Methyl (5-hydroxy-2,3-dihydro-1H-inden-1-yl)acetate Preparation Products And Raw materials |
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