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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646910Generated: November 1, 2026

Sodium Sulfite → (Z)-2-Carbomethoxy-3-phenyl-2-propene-1-sulfonic Acid Sodium Salt

https://huagongshe.com/reaction/1646910

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfiteHCID 24437—
ReactantPotassium BromideHCID 253877—
ReactantSodium BromideHCID 253881—
ReactantMethyl 2-(bromomethyl)-3-phenylacrylateHCID 5904127—
SolventMethanolHCID 887—
Product(Z)-2-Carbomethoxy-3-phenyl-2-propene-1-sulfonic Acid Sodium SaltHCID 88128861—

Reaction Conditions

Temperature50 °C

Reaction Steps

To a 12L, 3-neck round bottom flask fitted with a mechanical stirrer, thermometer and an addition funnel was added the resultant product from Example 3B (400 g, 1.57 mol) and methanol (4L). The mixture was warmed to 50° C. and a solution of sodium sulfite (199 g, 1.57 mol) dissolved in water (4L) was added over 75 min while the internal temperature of the flask was maintained at 50° C. After the addition was complete, the clear solution was allowed to stir at 50° C. for an additional 45 min. The reaction mixture in solution was taken to the next step without additional purification. The compound can be isolated by concentration to an amorphous powder, which is contaminated with an equivalent of sodium bromide: IR (KBr) 1711, 1628, 1215 cm-1 ; 1H NMR (DMSO D-6) delta 3.70 (s, 3H), 3.77 (s, 2H), 7.33-7.41 (m, 3H), 7.48 (s, 1H), 7.87-7.89 (m, 2H); 13C NMR (75 MHz, DMSO D-6) delta 49.88, 51.93, 127.36, 128.33, 128.91, 129.82, 134.75, 139.06, 168.60.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05182266
Source datasetuspto-grants-1993_01
ORD IDord-faf53b1c1c894e8aa60dddd57e40c7ca
Source noteuspto-grants-1993_01