HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25851Generated: October 26, 2026
tert-Butanol → (S)-1-Boc-3-isopropylpiperazine
https://huagongshe.com/reaction/25851
Participants
| Role | Name | HCID | Charge |
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| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Reactant | N-Benzyloxycarbonyl-valine glycine-methylester | HCID 69129945 | — |
| Solvent | Water | HCID 962 | — |
| Product | (S)-1-Boc-3-isopropylpiperazine | HCID 24820348 | 98.37% |
Reaction Steps
5.68 ml (14.20 mmol, 1.00 eq.) of a 2.5 N aq. NaOH-solution were added to a solution of 1.82 g (14.19 mmol) 2-(S)-Isopropyl-piperazine (82) in 70 ml tert-Butanol and 70 ml H2O. After cooling to 0° C. 3.10 g (14.20 mmol, 1.00 eq.) Boc-anhydride was added and the mixture was stirred at 0° C. for 1 h. Then the solution was warmed to r.t. and stirred overnight. After evaporating the tert-Butanol the mixture was extracted with CH2Cl2. The comb. org. fractions were dried over Na2SO4 and evaporated. Column chromatography (CH2Cl2/MeOH (10+1)) yielded 3.19 g (13.96 mmol, 98.37%) 3-(S)-Isopropyl-piperazine-1-carboxylic acid tert-butyl ester (85) as a clear oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06858600B2 |
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| Source dataset | uspto-grants-2005_02 |
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| ORD ID | ord-0d0f7fe44df34cb9916b0ca8ec7f9729 |
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| Source note | uspto-grants-2005_02 |
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