HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1407960Generated: October 30, 2026
Oxalyl chloride → Tert-butyl 3-(3-(chlorocarbonyl)benzylthio)propanoate
https://huagongshe.com/reaction/1407960
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-((3-Tert-butoxy-3-oxopropylthio)methyl)benzoic acid | HCID 66586713 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 3-(3-(chlorocarbonyl)benzylthio)propanoate | HCID 86705208 | — |
Reaction Steps
Into a 100-mL round-bottom flask, was placed a solution of 3-((3-tert-butoxy-3-oxopropylthio)methyl)benzoic acid 1.1c (3.00 g, 10.14 mmol, 1.00 equiv) in dichloromethane (50 mL). This was followed by the addition of oxalyl dichloride (4.50 g, 35.43 mmol, 3.00 equiv) dropwise with stirring at 0° C. To this was added N,N-dimethylformamide (one drop). The resulting solution was stirred for 1.5 h at room temperature. The resulting mixture was concentrated under vacuum. This resulted in 3.18 g (99%) of tert-butyl 3-(3-(chlorocarbonyl)benzylthio)propanoate as red oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08916569B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-61b9d039c855453ebe078f51c0169654 |
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| Source note | uspto-grants-2014_12 |
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