HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 734391Generated: October 31, 2026
Methyl iodide → (R)-2-(5-benzyloxy-indol-1-yl)-propionic acid methyl ester
https://huagongshe.com/reaction/734391
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | (R)-2-(5-benzyloxy-indol-1-yl)-propionic acid | HCID 57845433 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (R)-2-(5-benzyloxy-indol-1-yl)-propionic acid methyl ester | HCID 67241338 | 87% |
Reaction Steps
A suspension of (R)-2-(5-benzyloxy-indol-1-yl)-propionic acid (Example 4, 18.0 g, 0.061 mol), sodium bicarbonate (15.36 g, 0.183 mol), and iodomethane (11.40 mL, 0.183 mol) in DMF (164 mL) was stirred at rt for 20 h. The reaction was monitored by reverse phase HPLC. Upon completion, the reaction was quenched by pouring into ice/water (300 mL) followed by extracting with ethyl acetate (2×150 mL). The combined organic layer was washed with water (2×150 mL) and brine (150 mL) and was dried over anhydrous sodium sulfate. Filtration and concentration to dryness gave a crude oil which was purified by silica gel chromatography using 10-35% ethyl acetate/hexanes to give 16.38 g (87%) of (R)-2-(5-benzyloxy-indol-1-yl)-propionic acid methyl ester as an oil. 1H NMR (DMSO-d6) δ 7.45 (d, 2H), 7.38 (m, 3H), 7.30 (m, 2H), 7.13 (s, 1H), 6.82 (d, 1H), 6.38 (s, 1H), 5.41 (q, 1H), 5.08 (s, 2H), 3.60 (s, 3H), 1.70 (d, 3H); LC/MS (+esi) m/z 310.2 (M+H)+, RT 3.47 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07592361B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-7148bd65834242b88e8fbe9683f25512 |
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| Source note | uspto-grants-2009_09 |
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