Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Dibenzylphosphinic chloride | HCID 12809684 | — |
| Reactant | Dibenzylphosphite | HCID 21904359 | — |
| Reactant | HCID 70420509 | HCID 70420509 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 70419999 | HCID 70419999 | — |
Reaction Steps
2 g of L-phenylalanine-glycine methyl ester hydrochloride (7.4 mmoles) are put in suspension in 20 ml of anhydrous chloroform. 1.50 g of triethylamine (15 mmoles) are added. The solid enters into solution. The solution is cooled to 0° C. and 2.17 g (7.4 mmoles) of dibenzyl phosphoryl chloride freshly prepared from dibenzyl phosphite and sulfuryl chloride are added while stirring for 30 minutes. The mixture is allowed to stand for 20 hours at room temperature. The precipitate formed is filtered and the filtrate is washed in succession with 30 ml of 1N HCl, 20 ml of water, 20 ml of 10% bicarbonate, then 2×30 ml of water. The organic solution is dried on anhydrous Na2SO4 and evaporated under a vacuum. A pale yellow solid is obtained which is recrystallized in ethyl acetate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04738803 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-d57968be17c94004a1cce1ebea2dbe29 |
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| Source note | uspto-grants-1988_04 |
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