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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051998Generated: October 29, 2026

Methane → HCID 20185736, compound

https://huagongshe.com/reaction/2051998

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethaneHCID 297—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant3-(Hydroxyamino)propylphosphonic acidHCID 342170—
ReactantBistrimethylsilylacetamidHCID 11708267—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 20185736HCID 2018573626%

Reaction Steps

A mixture of 3-(N-hydroxyamino)propylphosphonic acid (820 mg), bis(trimethylsilyl)acetamide (5.0 g), triethylamine (1.01 g) and dichloromethane (40 ml) was stirred at ambient temperature for 2.5 hours. The reaction mixture was cooled to 0°-5° C. and mesyl chloride (1.15 g) was added dropwise with stirring. The reaction mixture was stirred for 1.25 hours and then concentrated under reduced pressure to give a residue, which was dissolved in water (50 ml). The solution was subjected to a column chromatography using activated charcoal. After the column was washed with water, the object compound was eluted with 70% aqueous acetone. The eluate was collected and evaporated to dryness to give powdery 3-(N-hydroxy-N-mesylamino)propylphosphonic acid (320 mg). This powder was dissolved in ethanol (20 ml). To the solution was added conc. aqueous ammonia (0.4 ml) to give precipitates, which were separated by filtration and dried to give crystalline monomammonium salt of 3-(N-hydroxy-N-mesylamino)propylphosphonic acid (220 mg). Mp 103°-105° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04182758
Source datasetuspto-grants-1980_01
ORD IDord-ec48a1a8589e43e884cd1ec965eb1502
Source noteuspto-grants-1980_01