HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1174376Generated: November 1, 2026
Triethylamine → tert-butyl 3-methyl-N-(methylsulfonyl)-L-valinate
https://huagongshe.com/reaction/1174376
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | L-(+)-Ttert-butyl tert-leuc-inate | HCID 11252445 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | tert-butyl 3-methyl-N-(methylsulfonyl)-L-valinate | HCID 86599586 | 100% |
Reaction Steps
A solution of tert-butyl 3-methyl-L-valinate (50 mg, 0.223 mmol) in dichloromethane (1 mL) at 0° C. was treated with 4-(dimethylamino)pyridine (5.4 mg, 0.045 mmol), triethylamine (93.4 μL, 0.67 mmol), and methanesulfonyl chloride (34.5 L, 0.45 mmol), and the mixture was warmed to 25° C. for 1 h. The mixture was washed with 5% potassium bisulfate, saturated sodium bicarbonate, brine, and dried over MgSO4, filtered, and the solvents were evaporated to give the crude title compound (59 mg, 100%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07834043B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-36a2dcb7615d4057b1f4c40e17389e13 |
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| Source note | uspto-grants-2010_11 |
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