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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2036200Generated: November 3, 2026

Potassium Carbonate → HCID 66653710, compound

https://huagongshe.com/reaction/2036200

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl (2S)-2-[(4-methylbenzene-1-sulfonyl)oxy]propanoateHCID 12884152—
ReactantHCID 66653819HCID 66653819—
SolventAcetonitrileHCID 6342—
ProductHCID 66653710HCID 66653710—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of (±)-1-(5-chloro-2-hydroxy-phenyl)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid benzyl ester (192 mg, 0.30 mmol, 1.0 eq.) in MeCN (1 mL), (S)-2-(toluene-4-sulfonyloxy)-propionic acid methyl ester (80 mg, 0.30 mmol, 1.0 eq.) and potassium carbonate anhydrous (83 mg, 0.60 mmol, 2.0 eq.) were added and the mixture was heated to 65° C. for 18 hours. (S)-2-(Toluene-4-sulfonyloxy)-propionic acid methyl ester (40 mg, 0.15 mmol, 0.5 eq.) was added again and the mixture was heated at 90° C. for 4 hours. The mixture was allowed to cool to r.t. and extracted with Et2O (2×), dried over MgSO4, filtered, and concentrated in vacuo. To a solution of the crude ester in THF (1.3 mL), 1M aq. NaOH soln. (0.38 mL) was added. The solution was stirred at r.t. for 18 hours. The solution was diluted with water (2 mL) and 1M aq. HCl soln. (0.38 mL) followed by DCM. The mixture was shaked then the layers were separated and the aq. phase was extracted with DCM (2×). The comb. org. phases were concentrated in vacuo. The crude mixture, redissolved in DMF (1.2 mL), was purified by prep. HPLC (column: Atlantis, 19×50 mm, 5 um, UV/MS, acidic conditions) to give the desired acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08575158B2
Source datasetuspto-grants-2013_11
ORD IDord-09794b7f4acd4b3aa379e9971a7b4a7e
Source noteuspto-grants-2013_11