HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 873701Generated: October 30, 2026
Chloroacetyl chloride → HCID 86724240, compound
https://huagongshe.com/reaction/873701
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloroacetyl chloride | HCID 6577 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 86724241 | HCID 86724241 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86724240 | HCID 86724240 | — |
Reaction Steps
To a mixture of (4-amino-6-bromo-4H-spiro[chromene-3,3′-oxetan]-4-yl)methanol (280 mg, 0.933 mmol), CH2Cl2 (10 mL) and saturated aqueous NaHCO3 (10 mL) was added a mixture of chloroacetyl chloride (0.083 mL, 1.02 mmol) and CH2Cl2 (1 mL) at ambient temperature. After stirring for 30 minutes at ambient temperature, chloroacetyl chloride (0.016 mL, 0.197 mmol) was added to the reaction mixture. The mixture was stirred for 10 minutes at ambient temperature, diluted with CH2Cl2 and separated. The organic layer was washed with water, dried over MgSO4 and filtered. Concentration of the filtrate at reduced pressure gave crude N-[6-bromo-4-(hydroxymethyl)-4H-spiro[chromene-3,3′-oxetan]-4-yl]-2-chloroacetamide, which was used for the next reaction without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08975415B2 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-3722d921743b4dd1876ac1351a8ac67a |
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| Source note | uspto-grants-2015_03 |
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