HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912427Generated: October 31, 2026
Water → [Benzyl-(2-chloropropyl)-amino]acetic acid tert-butyl ester
https://huagongshe.com/reaction/1912427
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | [Benzyl-(2-chloro-1-methylethyl)-amino]acetic acid tert-butyl ester | HCID 58293349 | — |
| Product | [Benzyl-(2-chloropropyl)-amino]acetic acid tert-butyl ester | HCID 58293274 | — |
Reaction Steps
An optically-active compound of [benzyl-(2-chloro-1-methylethyl)-amino]acetic acid tert-butyl ester (172.9 g) was dissolved in N,N-dimethylformamide (520 ml), and stirred at 80° C. for 140 minutes. The reaction mixture was cooled to 0° C. Then, thereto was added water (1200 ml), and the mixture was extracted with n-hexane/ethyl acetate (2/1, 1000 ml). The organic layer was sequentially washed with water (700 ml) and saturated aqueous sodium chloride solution (400 ml), and the separated aqueous layer was extracted with n-hexane/ethyl acetate (2/1, 600 ml) again. The combined organic layer was concentrated under reduced pressure, and the resulting residue was purified by silica gel column chromatography (eluent: n-hexane/ethyl acetate=50/1 to 40/1) to give the titled compound (127.0 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08609647B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-52cafdcaf7844865ac55bdbdd3f9af04 |
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| Source note | uspto-grants-2013_12 |
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