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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1872465Generated: November 1, 2026

Hydrochloric Acid → HCID 57225017, compound

https://huagongshe.com/reaction/1872465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantHCID 70076632HCID 70076632—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 57225017HCID 5722501773.2%

Reaction Conditions

Temperature23 °C

Reaction Steps

A solution of (1S,2R,3R,5R,6S)-2-amino-3-benzyloxy-bicyclo [3.1.0] hexane-2,6-dicarboxylic acid 2-benzyl ester 6-ethyl ester (XXIV-3) (50 mg, 0.122 mmol) and LiOH.H2O (13 mg, 0.30 mmol) in THF (4 mL), H2O (2 mL) and MeOH (0.4 mL) was stirred at 23° C. for 36 h. The solution was acidified with conc. HCl and evaporated to dryness. The remaining pale yellow solid was suspended in EtOH, filtered, washed with more EtOH and the filtrate was evaporated to dryness. The residue was dissolved in EtOH (1 mL) and propylene oxide (1 mL) and refluxed for 3 min, whereupon the amino acid precipiated. After cooling to 23° C., the product was filtered off, washed with ether and dried to give (1S,2R,3R,5R,6S)-2-amino-3-benzyloxybicyclo[3.1.0]hexane-2,6-dicarboxylic acid (I-10) (26 mg, 72%) as a white solid. 1H-NMR (250 MHz, D2O) □1.57 (1H, t, J=3.5 Hz), 1.97 (2H, m), 2.13 (1H, ddd, J=12.5, 8,3.5 Hz), 2.35 (1H, dd, J=12.5, 7 Hz), 3.73 (1H, dd, J=8, 7 Hz), 4.51 (2H, s), 7.36 (5H, bm); MS[ISN] 290 [(M-H)- ]; mp>250° C.; □D20 -5.69° (c=0.25, H2O).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06107342
Source datasetuspto-grants-2000_08
ORD IDord-94b47de4e41e4d628eba55b10c7d3e9c
Source noteuspto-grants-2000_08