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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1704184Generated: October 26, 2026

Carbon tetrabromide → dimethyl N-(5-isopropyl-2-morpholinophenyl)phosphoramidate

https://huagongshe.com/reaction/1704184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon tetrabromideHCID 11205—
ReactantSodium HydroxideHCID 14798—
ReactantDimethylphosphiteHCID 21884954—
ReactantHCID 22752981HCID 22752981—
CatalystBenzyl triethylammonium chlorideHCID 66133—
SolventDichloromethaneHCID 6344—
Productdimethyl N-(5-isopropyl-2-morpholinophenyl)phosphoramidateHCID 2275896437%

Reaction Steps

To a stirred solution of 10 ml. of methylene dichloride, 7 ml. of 20% aqueous sodium hydroxide, 3 g. of tetrabromomethane, and 0.2 g. of triethylbenzylammonium chloride was slowly added a solution of 4.0 g. (0.018 moles) of 4-(2-amino-4-isopropylphenyl)morpholine and 2.0 g. of dimethylphosphite dissolved in about 20 ml. of methylene dichloride. The reaction was exothermic and cooling by an ice bath was required. After stirring at ambient temperature for 18 hours, GC analysis indicated the reaction was about 30% complete. Accordingly, a 10% excess of the dimethylphosphite (0.2 g.) and an additional 0.3 g. of tetrabromomethane was added and stirring of the reaction mixture continued overnight. The mixture was then poured into an ice-water solution and the methylene dichloride layer separated. The aqueous layer was extracted twice with methylene dichloride and the combined methylene dichloride phases were rinsed thrice with water. After drying over anhydrous sodium sulfate, the methylene dichloride solution was filtered and evaporated under reduced pressure. The residue was eluted through a silica gel column using 99.5% methylene dichloride and 0.5% methanol to separate the product which was isolated from the solvent as a tan solid (2.2 g.; 37% yield); melting point 97°-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04126442
Source datasetuspto-grants-1978_11
ORD IDord-c0c2687655be4f74abac0118c492b41c
Source noteuspto-grants-1978_11