HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537628Generated: October 30, 2026
Hydrochloric Acid → Fmoc-D-Lys(Boc)-D-Lys(Boc)-Leu-Leu-OH
https://huagongshe.com/reaction/537628
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Fmoc-D-Lys(Boc)-D-Lys(Boc)-Leu-Leu-OBzl | HCID 131731956 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Solvent | Heptane | HCID 8900 | — |
| Product | Fmoc-D-Lys(Boc)-D-Lys(Boc)-Leu-Leu-OH | HCID 131731958 | 93% |
Reaction Steps
The crude crystals (1.23 g) of Fmoc-D-Lys(Boc)-D-Lys(Boc)-Leu-Leu-OBzl (2-MeO-4-OC12OC22) were dissolved in a mixture of chloroform (12 mL) and heptane (12 mL), and 3% trifluoroacetic acid/(chloroform-heptane=1:1) solution was added dropwise under ice-cooling. The reaction mixture was stirred in a water bath at 10-15° C. for 3 hr, and 2.5% aqueous sodium hydrogen carbonate solution (18 mL) and chloroform (18 mL) were added. 0.1N Hydrochloric acid was added, and the aqueous layer was adjusted to pH 2. The aqueous layer was removed, and the organic layer was washed 3 times with purified water (10 mL). The combined organic layers were concentrated under reduced pressure, and heptane (30 mL) was added to the residue. The precipitated crystals were washed at 40° C. and collected by filtration to give Fmoc-D-Lys(Boc)-D-Lys(Boc)-Leu-Leu-OH (800 mg, 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859732B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-820ea2c44316473b8c27c63d2d9eb66b |
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| Source note | uspto-grants-2014_10 |
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