HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1197927Generated: October 31, 2026
1,2-Dichloroethane → HCID 57180353, compound
https://huagongshe.com/reaction/1197927
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 57097436 | HCID 57097436 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57180353 | HCID 57180353 | 83.3% |
Reaction Steps
0.6 g (1.23 mmol) of 4-[[(2S,3S)-3-(1-t-butoxyformamido)-2-(t-butoxydimethylsiloxy)-3-(cyclohexylmethyl)propyl]amino]butyric acid was dissolved in 2 ml of methylene chloride and added dropwise at -20° to a solution of 285 mg of EDC and 200 mg of HOBT in 13 ml of methylene chloride. The reaction mixture was subsequently warmed to room temperature within 15 minutes, stirred at this temperature for 17 hours and subsequently poured into water and extracted with methylene chloride. The methylene chloride extracts were dried over magnesium sulfate, evaporated under reduced pressure and the residue was chromatographed on 10 g of silica gel using a mixture of methylene chloride and isopropanol as the eluting agent, whereby there were obtained 480 mg of t-butyl [(1S,2S)-2-(t-butyldimethylsiloxy)-1-(cyclohexylmethyl)-3-(2-oxo-1-pyrrolidinyl)propyl]carbamate as an oil which was used directly in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05278148 |
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| Source dataset | uspto-grants-1994_01 |
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| ORD ID | ord-38a8554eaa964671aff82ef1c240324a |
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| Source note | uspto-grants-1994_01 |
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