HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 891801Generated: October 29, 2026
3-Hydroxyazetidine → HCID 86590882, compound
https://huagongshe.com/reaction/891801
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Hydroxyazetidine | HCID 1514290 | — |
| Reactant | HCID 86590883 | HCID 86590883 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 86590882 | HCID 86590882 | 61% |
Reaction Steps
To a solution of 3-(t-butyldiphenylsilyloxy)-2-isothiocyanatopropionic acid methyl ester (13.4 g, 33.5 mmol) (obtained as described in Reference Example 70(1)) in tetrahydrofuran (245 ml) was added a solution of 3-hydroxyazetidine (4.90 g, 67.1 mmol) (obtained as described in Reference Example 31(1)) in water (50 ml) at room temperature and the mixture was stirred overnight. After checking the completion of the reaction, the reaction mixture was partitioned between ethyl acetate and saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by chromatography on a silica gel column using toluene and toluene:acetonitrile (3:1) as the eluant to afford (2S)-3-(t-butyldiphenylsilyloxy)-2-[(3-hydroxyazetidine-1-carbothioyl)amino]propionic acid methyl ester (9.60 g, yield 61%) as an yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07001897B2 |
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| Source dataset | uspto-grants-2006_02 |
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| ORD ID | ord-ae3948d98d2e441e84fa584781c0593c |
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| Source note | uspto-grants-2006_02 |
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