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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1781989Generated: October 25, 2026

Hydrochloric Acid → 2-Methoxyestra-1,3,5(10)-triene-3-ol

https://huagongshe.com/reaction/1781989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium HydroxideHCID 14797—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant2-MethoxyestroneHCID 440624—
SolventEthylene GlycolHCID 174—
Solvent1-ButanolHCID 263—
Product2-Methoxyestra-1,3,5(10)-triene-3-olHCID 4622737872%

Reaction Conditions

Temperature130 °C

Reaction Steps

2-Methoxyestrone (Scheme 1, Compound 4) (450 mg, 1.5 mmol) was suspended in ethylene glycol (10 mL) and n-butanol (2 mL). Hydrazine hydrate (0.145 mL, 3 mmol) was added and the mixture was heated to 130° C. for 1 h. The reaction was cooled to 70° C., KOH (253 mg, 4.5 mmol) was added, then the reaction was heated at 200° C. for 1 h. The mixture was cooled to room temperature, poured into ice and HCl (6N, 6 mL) was added. The resulting solid was filtered off. The solid was dissolved in acetone, which was then evaporated to give a product (Scheme 1, Compound 7) (310 mg, 72% yield). 1H NMR (300 MHz, CDCl3) δ 6.93 (1H, s, aromatic), 6.75 (1H, s, aromatic), 5.35 (1H, s, phenol), 3.95 (3H, s, methoxy), 2.95 (2H, dd, J=5.0, 3.0 Hz), 2.25 (2H, m,), 1.95 (2H, m), 1.95-1.05 (11H, m), 0.8 (3H, s)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07498322B2
Source datasetuspto-grants-2009_03
ORD IDord-b3178f60b4774d0b9e3efc65f3fe44ff
Source noteuspto-grants-2009_03