HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365886Generated: October 25, 2026
Sodium Bicarbonate → D-Homophenylalanine Benzyl ester
https://huagongshe.com/reaction/1365886
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | D-Homophenylalanine Benzyl ester Tosylate | HCID 86602419 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | D-Homophenylalanine Benzyl ester | HCID 15630399 | — |
Reaction Steps
D-Homophenylalanine Benzyl ester Tosylate (2.48 g, 5.6 mmol) was suspended in ethyl acetate (25 mL) and a saturated solution of sodium bicarbonate in water was added in portions (25 mL) with stirring at 25° C. The water layer was extracted with ethyl acetate (3×10 mL). The combined organic extract was dried over anhydrous sodium sulfate, filtered and concentrated to dryness to afford D-Homophenylalanine Benzyl ester. The ester was dissolved in acetonitile (25 mL). NaNd-bis-Boc-L-Ornithine (2.0 g, 6.0 mmol) was then added followed by N-hydroxysuccinimide (50 mg) and dicyclohexylcarbodiimide (1.28 g, 6.2 mmol). The reaction was stirred at 25° C. for 30 hr, filtered and the filtrate concentrated to dryness to afford crude product. It was purified by column chromatography on silica gel (hexane:ethyl acetate=3:1), which gave the title product (2.80 g) as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07893020B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-e1f3febee43941949c08619364c34604 |
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| Source note | uspto-grants-2011_02 |
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