HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430685Generated: October 30, 2026
4-Methylbenzoyl Chloride → N-p-toluoyl valinol
https://huagongshe.com/reaction/430685
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methylbenzoyl Chloride | HCID 13405 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Valinol | HCID 79019 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-p-toluoyl valinol | HCID 18346087 | 89.6% |
Reaction Steps
Diisopropylethyl amine (17.4 ml, 134 mmol) was added a solution of (DL)-valinol (9.85 g, 95 mmol) in methylene chloride (100 ml). The reaction mixture was cooled to 0 °C., treated with a solution of p-toluoyl chloride (12.8 ml, 91 mmol ) in methylene chloride (50 ml) and then allowed to warm to room temperature. After stirring for 3 hours, excess aqueous sodium hydroxide solution was added and the reaction was transferred to a separatory funnel. The organic layer was separated and the aqueous layer washed with one portion of methylene chloride. The combined organic layers were washed with water and brine, dried over magnesium sulfate and concentrated in vacuo. Chromatography eluting with 25% ethyl acetate in hexanes, followed by 50% ethyl acetate in hexanes gave N-p-toluoyl valinol (18.04 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06323223B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-3da5c5c438e144feae7f883e23a702ff |
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| Source note | uspto-grants-2001_11 |
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