HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973593Generated: October 29, 2026
Benzyl chloroformate → HCID 178523374, compound
https://huagongshe.com/reaction/973593
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzyl chloroformate | HCID 10387 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 3-Aminopropylphosphinic acid | HCID 121956 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178523374 | HCID 178523374 | — |
Reaction Steps
A solution of 5.0 g of 3-aminopropylphosphinic acid in 200 ml of water is cooled to 5°, and the pH adjusted to 9.5 with 2 molar sodium hydroxide solution. To this mixture is added 6.8 g of benzyl chloroformate whilst maintaining the pH and temperature. After the addition is complete the mixture is stirred for 3 hours at pH 9.5 at room temperature and left to stand overnight. The mixture is then extracted with 100 ml of ether and the aqueous layer stirred at 5° with an equal volume of chloroform. The mixture is acidified to pH 2, the chloroform layer separated, dried over magnesium sulfate and the solvent evaporated under reduced pressure. The oily product is triturated with ether to give a white solid, 3-(N-benzyloxycarbonylamino)propylphosphinic acid, m.p. 53°-55°, 31P-NMR : δ=+36.6 ppm (CDCl3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05064819 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-3bd951af2335472db6790ab97bc20427 |
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| Source note | uspto-grants-1991_11 |
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