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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421096Generated: November 1, 2026

Sodium Bicarbonate → Methyl 2-[(3,5-diaminophenyl)methoxy]acetate

https://huagongshe.com/reaction/1421096

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 15907745HCID 15907745—
SolventMethanolHCID 887—
ProductMethyl 2-[(3,5-diaminophenyl)methoxy]acetateHCID 1590774664.3%

Reaction Steps

A mixture of 2.1 (5.0 g, 18.5 mmol), SnCl2 dihydrate (48.0 g, 212.7 mmol) in 60 mL of methanol was refluxed for 40 minutes. The resulting dark solution was cooled (ice bath) and cautiously neutralized by adding saturated NaHCO3. The solid precipitate was filtered off and washed with methanol and CH2Cl2 until no product was found (by TLC) in the washings. The filtrate and washings were combined and evaporated in vacuo to give crude diamine 2.2. Chromatography on a silica gel column (4.5×20 cm) eluting with ethyl acetate afforded the title compound as a yellow oil (2.5 g, 64%), which slowly crystallized upon drying in vacuo: 1H NMR (CDCl3) δ 6.11 (d, J=2 Hz, 1H, C4 --H), 5.96 (t, J=2 Hz, 2H, C2 --H), 4.44 (s, 2H, CH2), 4.07 (s, 2H, CH2), 3.75 (s, 3H, CH3), 3.59 (br s, 4H, NH2); 13C NMR (CDCl3) δ 170.96, 147.78, 139.33, 105.51, 101.41, 73.31, 66.85, 51.89.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06072046
Source datasetuspto-grants-2000_06
ORD IDord-79bf03a9c57f48a3b63326bf04ef5b53
Source noteuspto-grants-2000_06