HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597675Generated: October 25, 2026
L-Isoleucine → tert-Butoxycarbonyl-L-isoleucine
https://huagongshe.com/reaction/597675
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Isoleucine | HCID 6306 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-tert-butoxycarbonyloxy-6-chloro-1H-benzotriazole | HCID 13292852 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | tert-Butoxycarbonyl-L-isoleucine | HCID 2724762 | 104.7% |
Reaction Steps
A suspension of 1-tert-butoxycarbonyloxy-6-chloro-1H-benzotriazole (2.7 g.), L-isoleucine (1.3 g) and triethylamine (3.5 ml.) in a mixture of water (8 ml.) and tert-butyl alcohol (12 ml.) was stirred for 2 hours at 60° to 62° C. tert-Butyl alcohol was distilled off from the reaction mixture under reduced pressure and water (15 ml.) was added to the residue. The mixture was adjusted to pH 3 with a citric acid aqueous solution under ice-cooling and extracted with ethyl acetate. The extract was then washed with water and a saturated sodium chloride aqueous solution. The thus formed precipitates were filtered off and then the filtrate was dried over magnesium sulfate. The solution was concentrated and a mixture of ether and petroleum ether (1:1) was added to the residue. An insoluble material was filtered off and the filtrate was concentrated under reduced pressure to give N-tert-butoxycarbonyl-L-isoleucine (2.4 g.), oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04014915 |
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| Source dataset | uspto-grants-1977_03 |
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| ORD ID | ord-406c3e8705d342ffaf86803df21e1f81 |
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| Source note | uspto-grants-1977_03 |
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