HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107113Generated: October 29, 2026
Piperidine → 3-(4-Methoxyphenylsulfanyl)-4-phenylbutyric acid
https://huagongshe.com/reaction/1107113
Participants
| Role | Name | HCID | Charge |
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| Reactant | Piperidine | HCID 8082 | — |
| Reactant | 4-Methoxybenzenethiol | HCID 12765 | — |
| Reactant | 4-Phenyl-2-butenoic acid | HCID 53401858 | — |
| Product | 3-(4-Methoxyphenylsulfanyl)-4-phenylbutyric acid | HCID 10638108 | 82% |
Reaction Steps
A mixture of 2 g (12.53 mmol) of 4-phenylbut-2-enoic acid, 1.8 mL (14.8 mmol) of 4-methoxybenzenethiol, and 0.4 mL (3.7 mmol) of piperidine is heated at 110° C. in a bomb for 18 hours. The reaction is partitioned between ethyl ether and 1N HCl. The organic layer is dried over anhydrous MgSO4 and concentrated in vacuo. Purification by flash silica gel chromatography affords 3.07 g (82%) of 3-(4-methoxyphenylsulfanyl)-4-phenylbutyric acid as a white crystalline solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06057369 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-46b1720d905f4b3b9480bf6bc7369970 |
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| Source note | uspto-grants-2000_05 |
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