HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30287Generated: October 29, 2026
Oxalyl chloride → HCID 86229119, compound
https://huagongshe.com/reaction/30287
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | HCID 67206550 | HCID 67206550 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86229119 | HCID 86229119 | — |
Reaction Steps
The product from step c) (1064 mg, 3.53 mmol) was dissolved in 20 mL of dichloromethane and cooled to 0° C. under N2 atmosphere and oxalyl chloride (1345 mg, 10.59 mmol) was added, followed by 2 drops of DMF. The reaction was stirred at 0° C. for 15 minutes and was allowed to come to room temperature. The reaction mixture was stirred for 1.5 hours and was evaporated to dryness to give the subtitle compound as a solid. MS calculated for C17H18ClNOS+H: 320, observed as methyl ester [dissolved in methanol]+H: 316.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423056B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-86e4200b507844be898358c1562c4fec |
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| Source note | uspto-grants-2008_09 |
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