HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 539625Generated: October 31, 2026
Trimethyl phosphonoacetate → HCID 67043500, compound
https://huagongshe.com/reaction/539625
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trimethyl phosphonoacetate | HCID 80029 | — |
| Reactant | Lithium Chloride | HCID 433294 | — |
| Reactant | HCID 58200258 | HCID 58200258 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Ammonium Chloride | HCID 25517 | — |
| Product | HCID 67043500 | HCID 67043500 | 81.6% |
Reaction Steps
To a stirring room temperature suspension of LiCl (0.84 g, 19.8 mmol) in dry acetonitrile (50 mL) was added trimethyl phosphonoacetate (4 mL, 24.75 mmol). The resulting mixture was stirred for 5 minutes, then TEA (2.76 mL, 19.8 mmol) was added. The reaction mixture was stirred for 10 minutes, and then a solution of (4-oxo-1-phenyl-butyl)-carbamic acid benzyl ester (16.5 mmol) in acetonitrile (15 mL) was added. The reaction mixture was stirred at room temperature for 18 hours, then diluted with diethyl ether and saturated aqueous NH4Cl. The organic layer was separated, washed with brine, dried over MgSO4, filtered and concentrated under reduced pressure to an oil, which was chromatographed (5%-40% EtOAc in hexanes) to give 4.41 g (79%) of 4-benzyloxycarbonylamino-4-phenyl-butyric acid methyl ester as a colorless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08871760B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-cbe3557726e34e04859247f4486392e3 |
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| Source note | uspto-grants-2014_10 |
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