HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250867Generated: October 31, 2026
Diisopropylethylamine → HCID 69922482, compound
https://huagongshe.com/reaction/1250867
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-(Trifluoromethyl)benzenesulfonyl chloride | HCID 2777399 | — |
| Reactant | 4-[4-((2S)-2-amino-2-tert-butoxycarbonyl-ethyl)-phenoxy]-butyric acid | HCID 69922785 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 69922482 | HCID 69922482 | — |
Reaction Steps
210.5 mg of 4-[4-((2S)-2-amino-2-tert-butoxycarbonyl-ethyl)-phenoxy]-butyric acid were dissolved in 2 ml of DMF and cooled to 0° C. 269 mg of 4-trifluoromethylbenzenesulfonyl chloride and 284 mg of diisopropylethylamine were added and the reaction mixture was stirred at 0° C. for 2 hours. The reaction mixture was cooled to −25° C. for 16 hours and then warmed to room temperature. The reaction was quenched by the addition of water, and the mixture was extracted three times with dichloromethane. The combined organic phases were dried with sodium sulfate, filtered and the solvent was removed in vacuo. The residue was chromatographed on silica gel eluting with dichloromethane/methanol/water/acetic acid (9/1/0.1/0.1). Yield 66 mg. MS (ES+): m/e=532.2 (M+H)+; 476.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06340679B1 |
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| Source dataset | uspto-grants-2002_01 |
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| ORD ID | ord-146753be332d496db88b17d58ef0b554 |
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| Source note | uspto-grants-2002_01 |
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