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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 904044Generated: October 29, 2026

Acetate → HCID 131711925, compound

https://huagongshe.com/reaction/904044

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetateHCID 175—
ReactantHCID 131711926HCID 131711926—
SolventWaterHCID 962—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 131711925HCID 131711925—

Reaction Steps

In 8 ml of trifluoroacetic acid is dissolved 200 mg of pGlu-Ala-Lys(Boc)-Ser-Gln-(D)-Leu-Gly-Ser-Asn-OBut and the solution is allowed to stand at room temperature for 60 minutes. The trifluoroacetic acid is distilled off under reduced pressure and the residue is precipitated with ether and recovered by filtration. The powders thus obtained are dissolved in a small amount of water and passed through a column of Amberlite IRA-410 (acetate-form) (1.5×7 cm). The effluent is combined with washings and lyophilized. The powdery lyophilizate is dissolved in a small amount of 1 N-acetic acid and put onto a chromatographic column of Sephadex LH-20(2.5×125 cm), elution being carried out with 1 N-acetic acid. The fractions from 190-205 ml are pooled and lyophilized. Yield 65 mg; [α]D22 -45.4° (c=0.4, H2O); Rf4 (Avicel)=0.37; amino acid analysis (acid hydrolyzate): Lys, 1.04(1); Asp, 0.98(1); Ser, 1.86 (2); Glu, 2.14(2); Gly, 0.93(1); Ala, 1.00(1); Leu, 1.00 (1); average recovery, 71.2%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04229438
Source datasetuspto-grants-1980_10
ORD IDord-fc9ec632ec4841ef9520d8673cf430a4
Source noteuspto-grants-1980_10