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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1647509Generated: November 1, 2026

Triethylamine → 3-(Tert-butyldimethylsilyloxymethyl)aniline

https://huagongshe.com/reaction/1647509

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)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05432194
Source datasetuspto-grants-1995_07
ORD IDord-77675cff1ce94d6bbddf48bd25d52a1b
Source noteuspto-grants-1995_07