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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854398Generated: November 1, 2026

Formaldehyde → HCID 22890942, compound

https://huagongshe.com/reaction/854398

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantTrimethyl phosphiteHCID 8472—
Reactant2-ThiophenesulfonamideHCID 72881—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
ProductHCID 22890942HCID 2289094234%

Reaction Conditions

Temperature55 °C

Reaction Steps

To a solution of 2-thiophenesulfonamide (vi) (1.0 g, 6.1 mmol) in methanol (5 mL) was added a catalytic amount of sodium methoxide and paraformaldehyde (200 mg, 6.7 mmol). The reaction was heated to 55° C. for 1 h, and then the homogeneous solution was cooled and trimethyl phosphite (0.8 mL, 6.8 mmol) was added. After heating the reaction mixture for an additional 1 h at 55° C., the reaction mixture was cooled and concentrated. The residue was dissolved in dichloromethane (15 mL), washed with water (10 mL), dried (MgSO4), filtered and concentrated. Purification by flash chromatography (elution with methanol-chloroform; 1:19) yielded (vii) (600 mg, 34%) as a colorless solid: 31P NMR: (162 MHz, CDCl3) δP 23.7. Also isolated was the corresponding N-methylated compound, [(2-thiophenesulfonyl-N-methylamino)methyl]-phosphonic acid dimethyl ester (234 mg, 13%) as a colorless solid: 3C NMR (100 MHz, CDCl3) δC 36.7, 44.6 (d, J=165 Hz), 53.2 (d, J=6.5 Hz), 127.6, 132.4, 132.6, 135.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07259172B2
Source datasetuspto-grants-2007_08
ORD IDord-cc1c5428fff040e7a346a9d5ffe2e42f
Source noteuspto-grants-2007_08