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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1975941Generated: October 31, 2026

HCID 131722532, compound → 1-(1,1-Dimethylethyl) 3-(carboxymethyl)-4-methoxybenzenepropanoate

https://huagongshe.com/reaction/1975941

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 131722532HCID 131722532—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product1-(1,1-Dimethylethyl) 3-(carboxymethyl)-4-methoxybenzenepropanoateHCID 21999894—

Reaction Steps

Methyl (Z)-5-t-butoxycarbonylvinyl-2-methoxyphenylacetate (250 mg, from above) in ethyl acetate (5 mL) in the presence of Pd/C (10% Pd content, 44 mg) was subjected to a Parr apparatus under 50 PSI of hydrogen gas for 1 hour. The mixture was filtered through celite and the filter cake washed with ethyl acetate. The filtrate and washing solution were combined and concentrated to give the desired product. 1H NMR (400 MHz, acetone-d6): δ 7.10 (d, 1H), 7.04 (s, 1H), 6.88 (d, 1H), 3.76 (s, 3H), 3.57 (s, 3H), 3.55 (s, 2H), 2.78 (t, 2H), 2.48 (t, 2H), 1.40 (s, 9H). This compound (100 mg) was then treated with LiOH monohydrate (27 mg) in ethanol/H2O (3:1, 4 mL) for 5 hours. The ethanol was evaporated on vacuo and the residual acidified to pH-1 and extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate and filtered. Concentration in vacuo afforded acid 10 (80 mg) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06225288B1
Source datasetuspto-grants-2001_05
ORD IDord-d68f983c9e99488d95032f56e302b8b5
Source noteuspto-grants-2001_05