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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982302Generated: October 28, 2026

Sodium Hydroxide → Boc-Pro-His-OH

https://huagongshe.com/reaction/1982302

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant1,2-Pyrrolidinedicarboxylic acid, 1-(1,1-dimethylethyl) 2-(2,5-dioxo-1-pyrrolidinyl) ester, (2S)-HCID 853883—
ReactantHCID 178419078HCID 178419078—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductBoc-Pro-His-OHHCID 178451947—

Reaction Steps

1.25 g of Boc-Pro-OSu [G. W. Anderson et al., J. Amer. Chem. Soc. 86, 1839 (1964)] and 0.68 g of H-His-OH are suspended in 4 ml of H2O and 2 ml of dioxan. While stirring vigorously, 2N NaOH is added by means of a pH stat at a pH value of 9.0. After 45 minutes the absorption of NaOH ceases. The now clear solution is stirred for a further 10 minutes, the pH value is adjusted subsequently to 5.0 with 4N HCl, and the whole is concentrated to approximately 5 ml. After the addition of 20 ml of H2O, the whole is again concentrated to approximately 5 ml and then purified by chromatography over a column of absorber resin, diaion HP-20 (φ=1.6 cm; length=20 cm). The bulk of this product is eluted with 20% isopropanol in H2O. The fractions that are pure according to thin layer chromatography are combined, concentrated almost to dryness and, after the addition of H2O, lyophilised, yielding Boc-Pro-His-OH in the form of an amorphous powder; Rf (E)=0.45; Rf (A)=0.21.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04595677
Source datasetuspto-grants-1986_06
ORD IDord-e4dcdf7b8eec43119defa4c35359598b
Source noteuspto-grants-1986_06