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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004851Generated: November 1, 2026

Hydrochloric Acid → HCID 10050846, compound

https://huagongshe.com/reaction/1004851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 10673801HCID 10673801—
ReactantButyllithiumHCID 178418339—
ProductHCID 10050846HCID 10050846—

Reaction Conditions

Temperature-78 °C

Reaction Steps

A 1.6 M solution of n-BuLi (17.5 mL) in hexanes was added dropwise by syringe under argon atmosphere at -78° C. to a solution of estradiol (4) (5.88 g, 11.2 mmol) in anhydrous THF (150 mL), and the resulting reaction mixture was stirred at -78° C. for 2 h. Anhydrous DMF (5.5 mL) was added and the stirring was continued for 1 h at -78° C. The mixture was warmed to 0° C. and stirred for 1 h, and poured onto an ice-cold solution of 3N HCl (100 mL). The aqueous layer was extracted with ether (3×300 mL). The combined organic layer was washed with 50% brine-water (100 mL), brine (150 mL), and dried over anhydrous sodium sulfate. The organic layer was filtered and evaporated under reduced pressure to afford impure estradiol (2), which was purified over a silica gel column using hexane-ethyl acetate as eluant. Appropriate fractions were combined and evaporated under reduced pressure to afford estradiol (2) (4.36 g, 82%): mp 145-147° C.; IR (KBr) 2920, 2820, 1675, 1600, 728, 685 cm-1, 1H NMR (CDCl3) δ 0.88 (s, 3H), 1.1-2.5 (m, 13H), 2.80-2.97 (m, 2H), 3.50 (t, J=8.5 Hz, 1H), 4.56 (s, 2H), 5.65 (s, 2H), 6.75 (s, 1H), 7.20-7.50 (m, 10H), 7.78 (s, 1H), 10.5 (s, 1H). Anal. (C34H40O3) C,H.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051726
Source datasetuspto-grants-2000_04
ORD IDord-9b5796d3803946fba1f05c7a582da7aa
Source noteuspto-grants-2000_04