HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 745906Generated: October 30, 2026
2-{[(Benzyloxy)carbonyl]oxy}-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione → HCID 53883501, compound
https://huagongshe.com/reaction/745906
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-{[(Benzyloxy)carbonyl]oxy}-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dione | HCID 93913 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 22828543 | HCID 22828543 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 53883501 | HCID 53883501 | 33.3% |
Reaction Steps
Sodium bicarbonate (4.2 g, 0.050 mol) and 5-hydroxylysine hydrochloride (2.50 g, 0.0126 mol) were dissolved in water (70 ml) with stirring at room temperature. Acetonitrile (40 ml) was added, followed by N-benzyloxycarbonyloxy-5-norbornen-2,3-dicarboximide (3.94 g, 0.0126 mol) in acetonitrile (30 ml) over 15 minutes. After 2 hours, most of the acetonitrile was removed in vacuo and the remaining solution was treated with hydrochloric acid to reduce the pH to 2.0. The solution was extracted with ethyl acetate (50 ml), the pH was increased to 5.5 with sodium hydroxide, and the product was purified over Dowex 50W-2X. The product was eluted with 3% pyridine in water, concentrated to a small volume and freeze dried to give III (1.24 g, 0.0042 mol, 33%); nmr (0.5 M NaOD in D2O)δ 1.4-2.1 (m, 4H, --CH2CH2 --), 3.1-3.5 (m, 2H, --NCH2CH ), 3.5-3.9 (m, 1H, --NCHRCO), 3.9-4.2 (m, 1H, --CH2CHOHCH2 --), 5.10 (s, 2H, --CH2O), 7.39 (s, 5H, --CH2O); mass spectrum (FAB): 297 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04602002 |
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| Source dataset | uspto-grants-1986_07 |
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| ORD ID | ord-8db4efba152645bbbab7dbd021fb4269 |
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| Source note | uspto-grants-1986_07 |
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