HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2425846Generated: October 30, 2026
Triethanolamine → (R)-1-(4-tert-butoxyphenyl)ethylamine
https://huagongshe.com/reaction/2425846
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethanolamine | HCID 7618 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-[(1R)-1-(4-tert-Butoxyphenyl)ethyl]-2-methoxyacetamide | HCID 67255626 | — |
| Solvent | Water | HCID 962 | — |
| Product | (R)-1-(4-tert-butoxyphenyl)ethylamine | HCID 29003336 | 73% |
Reaction Steps
(R)—N-1-(4-tert-Butoxyphenyl)ethylmethoxyacetamide from example 1.3 (180 g with a purity of 94%; corresponds to 0.64 mol of pure substance) was mixed with triethanolamine (20 ml) with stirring and then admixed with 50% NaOH (70.8 g, 0.89 mol). The mixture was then stirred at a bath temperature of 140° C. for another seven hours, after which all of the amide had been converted according to GC. The mixture was diluted with water (100 ml), cooled and extracted with tert-butyl methyl ether (3×100 ml). The combined extracts were washed with saturated sodium chloride solution (50 ml) and dried over Na2SO4. After the solvent had been removed on a rotary evaporator, 123.7 g (73%) of (R)-1-(4-tert-butoxyphenyl)ethylamine were obtained in the form of a pale brownish oil. The chemical purity was 99.4%, the optical purity 98.9% ee.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968328B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-cc9fb6da51cc42da9da4b1c2073b15d1 |
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| Source note | uspto-grants-2011_06 |
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