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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910604Generated: October 28, 2026

HCID 66910183, compound → HCID 66910132, compound

https://huagongshe.com/reaction/910604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66910183HCID 66910183—
ReactantHCID 66910196HCID 66910196—
CatalystHCID 178419074HCID 178419074—
SolventDichloromethaneHCID 6344—
ProductHCID 66910124HCID 66910124—
ProductHCID 66910132HCID 66910132100%

Reaction Steps

To a solution of 3β,17β-di(dimethyltert-butylsilyloxy)androstane-6α-ol and 3α,17β-di(dimethyltert-butylsilyloxy)androstane-6α-ol (90/10 mixture, 6.30 g) in CH2Cl2 (60 mL) under N2, NMNO (4.07 g), TPAP (0.412 g) and 4 Å molecular sieves (3.50 g) were added. The mixture was stirred for 2 h and then SiO2 was added. The mixture was purified by flash chromatography (SiO2, n-hexane/Et2O 50/50) to give 3β,17β-di(dimethyltert-butylsilyloxy)-androstane-6-one and 3α,17β-di(dimethyltert-butylsilyloxy)androstane-6-one (90/10 mixture, 6.30 g, 100%). 1H-NMR (300 MHz, DMSO-d6, ppm from TMS): δ 3.68 (m, 1H), 3.67-3.57 (m, 1H), 2.38-2.30 (m, 1H), 2.20-2.12 (m, 1H), 1.99-1.05 (m, 18H), 0.90 (s, 9H), 0.88 (s, 9H), 0.75 (s, 3H), 0.74 (s, 3H), 0.07-0.03 (s, 12H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022203B2
Source datasetuspto-grants-2011_09
ORD IDord-d43932d137e840c0b81656bf70a201de
Source noteuspto-grants-2011_09