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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110827Generated: October 27, 2026

2-[3-(2-Oxopropylsufonyl)-4-n-propoxy-5-benzyloxy-phenyl]-5-(3,4,5-trimethoxyphenyl) tetrahydrofuran → 2-[3-(2-Oxopropylsulfonyl)-4-n-propoxy 5-hydroxyphenyl]-5-(3,4,5-trimethoxyphenyl)tetrahydro-furan

https://huagongshe.com/reaction/1110827

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[3-(2-Oxopropylsufonyl)-4-n-propoxy-5-benzyloxy-phenyl]-5-(3,4,5-trimethoxyphenyl) tetrahydrofuranHCID 20067477—
CatalystAcetic AcidHCID 176—
CatalystPalladiumHCID 23938—
SolventEthyl AcetateHCID 8857—
Product2-[3-(2-Oxopropylsulfonyl)-4-n-propoxy 5-hydroxyphenyl]-5-(3,4,5-trimethoxyphenyl)tetrahydro-furanHCID 19899146—

Reaction Steps

A mixture of 1.2 g of 2-[3-(2-oxopropylsufonyl)-4-n-propoxy-5-benzyloxy- phenyl]-5-(3,4,5-trimethoxyphenyl) tetrahydrofuran, 400 mg 10% Pd/C, 1-2 drops of acetic acid in 100 mL of ethyl acetate was stirred under H2 at 40 psi for 45 minutes. The reaction mixture was filtered over a bed of celite and evaporated in vacuo to yield the title compound: NMR(200 MHz, CDCl3) δ 1.10 (t, CH2CH2CH3), 1.92 (m, CH2CH2CH3), 1.9-2.6 (m, 3-CH2 & 4-CH2), 2.40 (s, CH3C(O)CH2), 3.86 (s, OCH3), 3.90 (s, 2 OCH3), 4.12 (t, OCH2CH2CH3), 4.42 (s, CH3C(O)CH2), 5.10-5.28 (m, 2-CH & 5-CH), 6.64 (s, 5-ArH), 7.35 & 7.47(2 d, 2-ArH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04977146
Source datasetuspto-grants-1990_12
ORD IDord-14763611064843f8adcc3d65dafa9b9a
Source noteuspto-grants-1990_12