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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1731967Generated: October 26, 2026

Trichloroacetic Acid → 2-[2-(bis-(2-chloroethyl)-amino)-6-methyl-2-oxo-tetrahydro-2H-1,3,2-oxazaphosphorin-4-yl-thio]-ethanesulphonic acid cyclohexylammonium salt

https://huagongshe.com/reaction/1731967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrichloroacetic AcidHCID 6421—
Reactant2-Sulfanylethane-1-sulfonic acid--cyclohexanamine (1/1)HCID 23049873—
Reactant2-(bis-(2-chloroethyl)-amino)-4-hydroxy-6-methyl-tetrahydro-2H-1,3,2-oxazaphosphorin-2-oxideHCID 23049875—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
Product2-[2-(bis-(2-chloroethyl)-amino)-6-methyl-2-oxo-tetrahydro-2H-1,3,2-oxazaphosphorin-4-yl-thio]-ethanesulphonic acid cyclohexylammonium saltHCID 131714975—

Reaction Steps

1.45 g (5 mmol) of 2-(bis-(2-chloroethyl)-amino)-4-hydroxy-6-methyl-tetrahydro-2H-1,3,2-oxazaphosphorin-2-oxide and 1.2 g (5 mmol) of cyclohexylammonium-2-mercaptoethanesulphonate were dissolved in 5 ml of water and in 5 ml of acetone, acidified with trichloroacetic acid and left to stand for 20 hours at 0° C. The mixture was then filtered, the filtrate was carefully concentrated under vacuum, the residue was taken up twice in acetone and was concentrated. The residue was then dissolved in acetone, precipitated with ether, and washed with ether and dried.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04623742
Source datasetuspto-grants-1986_11
ORD IDord-350e79586f1941ef8f389983802a67bf
Source noteuspto-grants-1986_11