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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375094Generated: October 30, 2026

Triethylamine → 3-(Tert-butyldimethylsilyloxymethyl)aniline

https://huagongshe.com/reaction/375094

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant3-Aminobenzyl alcoholHCID 80293—
SolventDichloromethaneHCID 6344—
Product3-(Tert-butyldimethylsilyloxymethyl)anilineHCID 1058597757%

Reaction Steps

To a solution of 3-aminobenzyl alcohol (2.00 g, 16.2 mmol) and tert-butyldimethylsilyl chloride (2.90 g, 19.4 mmol) in CH2Cl2 (32.5 mL) was added triethylamine (7.45 mL, 53.5 mmol). The reaction mixture was stirred for 18 hours at ambient temperature and was then partitioned between ethyl acetate and H2O. The organic phase was washed twice with H2O, twice with brine, dried over MgSO4, filtered, and concentrated in vacuo. 3-(O-t-butyldimethylsilyloxymethyl)aniline (2.18 g, 57%) was obtained as a yellow oil by chromatography on silica gel (30% ethyl acetate/hexane). 1H NMR (300 MHz, CDCl3) δ7.10 (1H, t, J=7.5 Hz), 6.67-6.72 (2H, m), 6.56 (1H, br d, J=7.5 Hz), 4.66 (2H, s), 3.63 (2H, br s), 0.94 (9H, s), 0.09 (6H, s). MS m/e 238 (M+H)+, 255 (M+NH4)30 .

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05484786
Source datasetuspto-grants-1996_01
ORD IDord-8a5fb12826ff43bba47963cb097984d0
Source noteuspto-grants-1996_01