HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264278Generated: October 25, 2026
4-Methoxybenzenesulfonyl chloride → N-[4-methoxybenzenesulfonyl]-(D)-valine
https://huagongshe.com/reaction/264278
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Methoxybenzenesulfonyl chloride | HCID 7401 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | D-Valine | HCID 71563 | — |
| Reactant | 1,4-Dioxane--water (1/1) | HCID 21886435 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-[4-methoxybenzenesulfonyl]-(D)-valine | HCID 1133588 | — |
Reaction Steps
To a solution of D-valine (15.0 g, 128.0 mmol) in 1:1 dioxane/water (200 mL) containing triethylamine (19.4 g, 192.0 mmol) at room temperature is added 4-methoxybenzene-sulfonyl chloride (29.0 g, 141.0 mmol), and the reaction mixture is stirred at room temperature overnight. The mixture is then diluted with methylene chloride, washed with 1N aqueous hydrochloric acid and water. The organic layer is washed again with brine, dried (Na2SO4), and the solvent is evaporated to provide N-[4-methoxybenzenesulfonyl]-(D)-valine as a crude product. A solution of this crude product (15.0 g) in toluene (100 mL) containing N,N-dimethylformamide di-t-butyl acetal (50 mL, 206.5 mmol) is heated to 95° C. for 3 hours. The solvent is then evaporated. The crude product is purified by silica gel chromatography (30% ethyl acetate/hexanes) to provide N-[4-methoxybenzene-sulfonyl]-(D)-valine t-butyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05646167 |
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| Source dataset | uspto-grants-1997_07 |
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| ORD ID | ord-94c9da312d5f43789f00688d9c9edd22 |
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| Source note | uspto-grants-1997_07 |
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