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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-{[(Benzyloxy)carbonyl]oxy}-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindole-1,3(2H)-dioneHCID 93913—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 22828543HCID 22828543—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 53883501HCID 5388350133.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04602002
Source datasetuspto-grants-1986_07
ORD IDord-8db4efba152645bbbab7dbd021fb4269
Source noteuspto-grants-1986_07