HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1092994Generated: November 2, 2026
1-Chloroethyl chloroformate → 3-((Tert-butyldiphenylsilyl)oxy)azetidine
https://huagongshe.com/reaction/1092994
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | 1-Benzhydryl-3-(tert-butyldiphenylsilyloxy)azetidine | HCID 17842412 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | 3-((Tert-butyldiphenylsilyl)oxy)azetidine | HCID 17842531 | — |
Reaction Steps
A stirred solution of 1-benzhydryl-3-(tert-butyl-diphenyl-silanyloxy)-azetidine (162a) (4.0 g, 8.4 mmol) in DCE (60 ml) at room temperature is treated with 1-chloroethylchloroformate (1.2 ml, 10.9 mmol) and the reaction mixture is heated to 80° C. After 2 hours, the solvent is removed in vacuo and the residue is dissolved in methanol (60 ml) and heated to reflux. After 1 h the reaction mixture is poured into water (250 ml), acidified with hydrochloric acid (1M solution) and washed with EtOAc (3×75 ml). The aqueous solution is basified with saturated sodium bicarbonate solution and extracted with EtOAc (3×75 ml). The combined organic layers are washed with water (2×50 ml), brine (50 ml), dried over MgSO4. The solvent is removed in vacuo to yield the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129541B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-c95ae3b4b4b54f868d3c8741123dcc10 |
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| Source note | uspto-grants-2012_03 |
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