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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2307471Generated: November 2, 2026

Methoxyacetic Acid → HCID 69919575, compound

https://huagongshe.com/reaction/2307471

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxyacetic AcidHCID 12251—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 69850326HCID 69850326—
ProductHCID 69919575HCID 6991957566%

Reaction Conditions

Temperature23 °C

Reaction Steps

To a stirred solution of 3-phenyl-N-[1-(1,2,3,4-tetrahydro-quinolin-7-yl)ethyl]acrylamide (Example 233) (75 mg, 0.245 mmol) in methoxyacetic acid (5 ml) was added, in small portions, NaBH4 (232 mg) over 30 minutes. The mixture was stirred at 23° C. for an additional 2 hours and then the excess hydride destroyed by adding MeOH. That solution was diluted with EtOAc and washed several times with water. The organic phase was dried (MgSO4) and evaporated. The crude material was purified by chromatography (SiO2, 25% EtOAc in hexane) yielding 59 mg (66%) of the desired compound as a thick oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06831080B2
Source datasetuspto-grants-2004_12
ORD IDord-ede1a26a4fa249c78796e6a141fc83f0
Source noteuspto-grants-2004_12