Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2216446Generated: October 31, 2026

Water → HCID 12132838, compound

https://huagongshe.com/reaction/2216446

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantSodium BicarbonateHCID 516892—
Reactant(2S)-2-[(1S)-5-methoxy-2,3-dihydro-1H-inden-1-yl]butanoic AcidHCID 11345339—
SolventDimethylformamideHCID 6228—
ProductHCID 12132838HCID 1213283899.8%

Reaction Steps

A suspension of acid prepared in Example 4 (220.0 g, 0.94 mol), NaHCO3 (237.0 g, 2.82 mol), CH3I (200 g, 1.41 mol) in 2.0 L DMF was stirred under Ar at rt for 18 hours. NMR analysis showed 95% reaction. Adding CH3I (100 g), and stirring for additional 24 hours at rt caused completion of the reaction. The reaction mixture was poured into 4.0 L water, and extracted with EtOAc (2×2 L). The organic layer was sequentially washed with water (2×1 L), 1 L of 1N NaOH solution, water (2×1 L), and 500 mL brine, and dried over Na2SO4. The product (233 g, 99%) was obtained as a light yellow oil after solvent removal and vacuum drying. 1H NMR (DMSO-d6) δ 6.90(d, 1H), 6.78(d, 1H), 6.66(dd, 1H), 3.70(s, 3H), 3.60(s, 3H), 3.20(m, 1H), 2.80(m, 2H), 2.40(m, 1H), 2.08(m, 1H), 1.80(m, 1H), 1.58(m, 1H), 1.40(m, 1H), 0.80(t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07112597B2
Source datasetuspto-grants-2006_09
ORD IDord-42611fc650eb4fd4a2d8fba5adec8c66
Source noteuspto-grants-2006_09