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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1816486Generated: October 30, 2026

Aniline → 3beta-tert-Butyldimethylsilyloxy-4,4-dimethyl-24-phenylamino-5alpha-chola-8,14-dien

https://huagongshe.com/reaction/1816486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant3beta-Tert-butyidimethylsilyloxy-4,4-dimethyl-5alpha-chola-8,14-dien-24 oic acidHCID 69410795—
SolventTetrahydrofuranHCID 8028—
Product3beta-tert-Butyldimethylsilyloxy-4,4-dimethyl-24-phenylamino-5alpha-chola-8,14-dienHCID 69411663—

Reaction Steps

3β-tert-Butyldimethylsilyloxy-4,4-dimethyl-5α-chola-8,14-dien-24 oic acid (0.15 g) is reacted with aniline following the procedure outlined in example 10 and reduced with lithium aluminium hydride (0.15 g) in THF at room temperature. Aqueous work-up and crystallization from methanol gives 3β-tert-butyldimethylsilyloxy-4,4-dimethyl-24-phenylamino-5α-chola-8,14-dien (106 mg). 1H-NMR (CDCl3, 300 MHz)): δ=7.17 (2H, t); 6.69 (1H, t); 6.6 (2H, d); 5.35 (1H, s); 3.6 (1H, s); 3.2 (1H, m); 3.09 (2H, m); 0.9 (9H, s); 0.04 (6H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06884796B2
Source datasetuspto-grants-2005_04
ORD IDord-e536b6abb53f43a199131a0aa9617387
Source noteuspto-grants-2005_04