HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777Generated: October 29, 2026
Thionyl Chloride → HCID 13927511, compound
https://huagongshe.com/reaction/1777
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Chloro-4-methoxycarbonyl valeric acid | HCID 86752220 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 13927511 | HCID 13927511 | — |
Reaction Steps
A mixture of 7.6 g of 2-chloro-4-methoxycarbonyl valeric acid, 9.2 ml of thionyl chloride and 30 ml of toluene was stirred for 30 minutes at 80° C., followed by distilling off the solvent under reduced pressure to leave 2-chloro-4-methoxycarbonyl butyryl chloride. A mixture of this compound, 5.0 g of 2-benzylaminobenzophenone, 100 ml of ethyl acetate and 100 ml of a saturated aqueous solution of sodium hydrogencarbonate was stirred for 30 minutes at room temperature. The ethyl acetate layer was washed with water and dried over anhydrous magnesium sulfate, then the solvent was distilled off under reduced pressure. The residue was purified by means of a silica gel column chromatography (eluent, hexane:ethyl acetate=5:1) to give 1.2 g of 2-[N-benzyl-N-(2-chloro-4-methoxycarbonyl)butyryl]aminobenzophenone as an oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05726306 |
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| Source dataset | uspto-grants-1998_03 |
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| ORD ID | ord-9645ae5ef13440c58b9e8e3877a34a9d |
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| Source note | uspto-grants-1998_03 |
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