HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 635778Generated: October 29, 2026
Sodium Bicarbonate → HCID 12794729, compound
https://huagongshe.com/reaction/635778
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-Formyl-2-hydroxybenzoic acid | HCID 656876 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 12794729 | HCID 12794729 | — |
Reaction Steps
Sodium cyanoborohydride (32 mg; 0.5 mmol) was added to a mixture of PAMAM 4.0 (EDA) (69 mg; 0.01 mmol), 4-formyl-2-hydroxybenzoic acid (83 mg; 0.5 mmol), and sodium hydrogen carbonate (42 mg; 0.5 mmol) in water (4 ml). The inhomogeneous orange mixture was stirred for four hours at room temperature, during which time it became homogeneous. The orange solution was then concentrated and the residue purified by gel filtration (Sephadex LH20; water) to give PAMAM 4.0 (EDA) terminated with ca. 32 4-carboxy-3-hydroxybenzylamine groups (91 mg). 1H and 13C nmr (D2O) shows mostly mono alkylation but with some signs of dialkylation of the terminal amino groups, both spectra show broad peaks. 13C nmr (D2O):δ 37.0; 41.1; 50.9; 53.4; 55.5; 55.8; 61.5; 120.9; 122.2; 122.4; 132.3; 132.7; 135.0; 135.8; 163.5; 163.7; 169.0; 178.6; 179.3. 1H nmr (D2O): δ 2.20; 2.35; 2.60; 3.15; 3.30; 3.55; 4.25; 6.68; 7.12; 7.55.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06190650B1 |
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| Source dataset | uspto-grants-2001_02 |
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| ORD ID | ord-65bcf918e16c4f5ebcc56eac5d8938a2 |
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| Source note | uspto-grants-2001_02 |
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