HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 867636Generated: October 31, 2026
Potassium Phosphate, Tribasic → 3-Methoxy-2-oxo-3-[[(phenylmethoxy)carbonyl]amino]-1-azetidinesulfonic acid, tetrabutylammonium salt
https://huagongshe.com/reaction/867636
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | Lithium methanolate | HCID 4177230 | — |
| Reactant | 2-Oxo-3-[N-chloro-N-[(phenylmethoxy)carbonyl]amino]-1-azetidinesulfonic acid, tetrabutylammonium salt | HCID 131714268 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Methoxy-2-oxo-3-[[(phenylmethoxy)carbonyl]amino]-1-azetidinesulfonic acid, tetrabutylammonium salt | HCID 131714266 | — |
Reaction Steps
To a stirring solution of lithium methoxide (667 mg) in anhydrous methanol (10 ml) at -78° C. is added a solution of 2-oxo-3-[N-chloro-N-[(phenylmethoxy)carbonyl]amino]-1-azetidinesulfonic acid, tetrabutylammonium salt (0.94 g) in dry dimethylformamide (10 ml). After stirring the mixture at -78° C. for 1 hour, it is poured into 0.5M monobasic potassium phosphate solution and extracted with methylene chloride (three 150 ml portions). The combined extracts are dried (sodium sulfate) and solvent is removed in vacuo to given an oil (0.83 g). The desired product is obtained by chromatographing the oil on silica gel (100 g) and eluting with 4-5% methanol in methylene chloride to give an oil (513 mg): λmax (neat) 1767, 1720 cm-1 ; NMR (CDCl3) δ 3.40 (S, OCH3), 3.03 (ABq, J=6.5 Hz, H4), 5.08 (S, CH2), 6.00 (S, NH), 7.27 (S, aromatic).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04775670 |
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| Source dataset | uspto-grants-1988_10 |
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| ORD ID | ord-6e65d52976d244348dfcf91b7cc877f4 |
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| Source note | uspto-grants-1988_10 |
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