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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171237Generated: October 28, 2026

Hydrochloric Acid → HCID 86621599, compound

https://huagongshe.com/reaction/1171237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantHCID 25066684HCID 25066684—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86621599HCID 8662159998%

Reaction Steps

(1R)-1-Methyl-2-phenylcarbonyloxyethyl(2S)-2-[(tert-butoxy)carbonylamino]-3-[3,4-bis(2,2-dimethylpropanoyloxy)phenyl]propanoate (13) (1.03 g, 1.64 mmol) was dissolved in 20 mL of 4M HCl in dioxane. The reaction mixture was stirred at room temperature for 60 min. Dioxane was completely evaporated under reduced pressure. The resulting white solid was dissolved in water (15 mL) and washed with methyl tert-butyl ether. The aqueous phase was collected and mixed with acetonitrile (10 mL). Lyophilization gave the title compound (12) (0.851 g, 98% yield) as a white solid. 1H NMR (400 MHz, CD3OD): δ 1.30 (3H, d, J=6.4 Hz), 1.33 (9H, s), 1.34 (9H, s), 3.13 (1H, dd, J=14.4, 6.8 Hz), 3.20 (1H, dd, J=14.4, 6.4 Hz), 4.22 (1H, t, J=6.8 Hz), 4.32 (1H, dd, J=12.4, 6.4 Hz), 4.49 (1H, dd, J=12, 3.2 Hz), 5.33 (1H, m), 7.10 (1H, d, J=8 Hz), 7.11 (1H, d, J=2 Hz), 7.17 (1H, dd, J=2, 8 Hz), 7.47 (2H, t, J=7.2 Hz), 7.58 (1H, t, J=7.2 Hz), 8.02 (2H, d, J=7.6 Hz). MS (ESI) m/z 528.14 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829592B2
Source datasetuspto-grants-2010_11
ORD IDord-308f7ce00f364f2aa1664261339e3e25
Source noteuspto-grants-2010_11