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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 861647Generated: October 30, 2026

Carbon Dioxide → HCID 45100640, compound

https://huagongshe.com/reaction/861647

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon DioxideHCID 280—
ReactantMethyl iodideHCID 6328—
ReactantDiisopropylamineHCID 7912—
Reactant3-Methylandrost-5-en-17-oneHCID 128915—
ReactantButyllithiumHCID 178418339—
SolventCarbon TetrachlorideHCID 5943—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
ProductHCID 45100640HCID 4510064074%

Reaction Steps

Diisopropyl amine (1.165 g, 11.5 mmol) was dissolved in dry tetrahydrofuran (30 mL) at -78° C. under N2. n-Butyl lithium (4.44 mL of a 2.6M solution in hexane, 11.5 mmol) was added via syringe and the solution warmed to -23° C. (CO2, CCl4) for 0.25 h. 3β-Methylandrost-5-en-17-one (3.0 g, 10.4 mmol) in dry tetrahydrofuran (30 mL) was added via syringe and the solution stirred for 0.25 h. Methyl iodide (7.0 g, 49.33 mmol) in dry tetrahydrofuran (30 mL) was added dropwise and the mixture stirred at room temperature for 1.5 h. The solution was quenched with saturated ammonium chloride and the organic layer separated, dried over magnesium sulfate, filtered, and evaporated. The residual solid was chromatographed on flash silica gel (120 g) and eluted with 1/99 (v/v) ether hexane to give 3β,16α-dimethylandrost-5-en-17-one (2.32 g, 74%). mp 109°-110° C. (recrystallized from methanol); NMR (CDCl3) δ 5.29 (br s, J=5 Hz, 1H, H-6), 2.52 (m, 1-H, H-16), 1.07 (d J=8 Hz, 3H, C-16 Me), 0.99 (s, 3H, C-19 Me), 0.91 (s, 3H, C-18 Me); IR (KBr) 2900, 1730, 1450, 1430, 1370; MS 300 (M+, 100), 285(62), 282(2), 272(12), 267(17), 229(20), 217(30), 159(17); Anal. Calcd for C21H32O: C, 83.93; H, 10.73. Found: C, 83.79; H, 10.52.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05714481
Source datasetuspto-grants-1998_02
ORD IDord-70c5ea8a8eff438ea27a18e2bab05d2b
Source noteuspto-grants-1998_02