HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237437Generated: October 30, 2026
1-Chloroethyl chloroformate → HCID 68468807, compound
https://huagongshe.com/reaction/2237437
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | HCID 58256121 | HCID 58256121 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | 1,1-Dichloroethane | HCID 6365 | — |
| Product | HCID 68468807 | HCID 68468807 | 54% |
Reaction Steps
A solution of the product from step g) (727 mg, 2.33 mmol) in anhydrous dichloroethane (11.6 ml) was cooled to 0° C., treated with 1-Chloroethyl chloroformate (1.27 ml, 11.65 mmol) and the reaction was warmed to 22° C. for 1 hour. The reaction diluted with CH2Cl2 (50 ml) and washed with sat. NaHCO3 (25 ml). The sat. NaHCO3 was back extracted with CH2Cl2 and the combined organic layers were washed with brine (25 ml), dried (MgSO4) and concentrated providing an oily residue, which was taken up in anhydrous MeOH (75 ml) and refluxed for 1 hour. The MeOH was evaporated and the crude residue was triturated with ether and filtered providing 323 mg (54%) of the subtitle compound. 1H NMR (300 MHz, DMSO) δ 9.60 (br s, 2H); 3.14-3.28 (m, 6H); 2.97-3.50 (m, 2H); MS: ESI (positive): 222, 224 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07718647B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-47fed3f43d0c4826bf0d86082a9fe136 |
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| Source note | uspto-grants-2010_05 |
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