HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375094Generated: October 30, 2026
Triethylamine → 3-(Tert-butyldimethylsilyloxymethyl)aniline
https://huagongshe.com/reaction/375094
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyldimethylsilyl chloride | HCID 28928 | — |
| Reactant | 3-Aminobenzyl alcohol | HCID 80293 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-(Tert-butyldimethylsilyloxymethyl)aniline | HCID 10585977 | 57% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05484786 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-8a5fb12826ff43bba47963cb097984d0 |
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| Source note | uspto-grants-1996_01 |
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