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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium BicarbonateHCID 516892—
Reactant(R)-2-(5-benzyloxy-indol-1-yl)-propionic acidHCID 57845433—
SolventDimethylformamideHCID 6228—
Product(R)-2-(5-benzyloxy-indol-1-yl)-propionic acid methyl esterHCID 6724133887%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07592361B2
Source datasetuspto-grants-2009_09
ORD IDord-7148bd65834242b88e8fbe9683f25512
Source noteuspto-grants-2009_09