HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1897480Generated: October 30, 2026
Dimethylamine → (S)-2-tert-Butoxycarbonylamino-4-dimethylaminobutyric acid methyl ester
https://huagongshe.com/reaction/1897480
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl (S)-2-(Boc-amino)-4-bromobutyrate | HCID 10685328 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (S)-2-tert-Butoxycarbonylamino-4-dimethylaminobutyric acid methyl ester | HCID 58797296 | 97% |
Reaction Steps
To a solution of (S)-4-bromo-2-tert-butoxycarbonylamino-butyric acid methyl ester (27.5 g, 93 mmol) in THF (100 mL) in a pressure reaction vessel was added triethylamine (26 mL) and dimethylamine (93 mL of 2.0 M in THF). The reaction vessel was sealed and heated to 60° C. for 16 hours and then cooled to room temperature. The reaction mixture was concentrated under reduced pressure and then dissolved in dichloromethane (500 mL). The solution was washed with water (3×200 mL) and brine (200 mL), dried over MgSO4, filtered through Celite and concentrated under reduced pressure. The residue was dried under high vacuum to afford 23.4 g of yellow oil (97% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08518983B2 |
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| Source dataset | uspto-grants-2013_08 |
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| ORD ID | ord-349ba96b543d427eab3e13b534e2790b |
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| Source note | uspto-grants-2013_08 |
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