HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 528738Generated: October 26, 2026
1,2-Dichloroethane → 3-Benzothiazol-2-yl-azetidine-1-carboxylic acid tert-butyl ester
https://huagongshe.com/reaction/528738
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Phosphorus oxide (P4O10) | HCID 14812 | — |
| Reactant | 1-Boc-Azetidine-3-carboxylic acid | HCID 2755981 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-Benzothiazol-2-yl-azetidine-1-carboxylic acid tert-butyl ester | HCID 44239818 | — |
Reaction Steps
To 10 mL DCE was added 533 mg (3.7 mmol) phosphorus pentoxide and 1.57 mL (7.36 mmol) bis-trimethylsilyl ether and the mixture was heated at 80° C. for 15 minutes. 0.19 g (0.92 mmol) N-boc-azetidine-3-carboxylic acid and 108 μL (1.01 mmol) 2-aminothiophenol were added and the mixture heated at 85° C. for 20 minutes. After cooling to room temperature the mixture was diluted with 20 mL DCM and washed with 1 M Na2CO3 (2×10 mL). The organic layer was dried with Na2SO4. After filtration and evaporation of the solvent the product was purified by column chromatography (silica, hexane/EtOAc 1:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09346816B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-14dc457f9ef24184930aed9bc7ae42b9 |
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| Source note | uspto-grants-2016_05 |
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