HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912426Generated: October 31, 2026
Thionyl Chloride → [Benzyl-(2-chloro-1-methylethyl)-amino]acetic acid tert-butyl ester
https://huagongshe.com/reaction/1912426
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | [Benzyl-(2-hydroxy-1-methylethyl)-amino]acetic acid tert-butyl ester | HCID 58293285 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | [Benzyl-(2-chloro-1-methylethyl)-amino]acetic acid tert-butyl ester | HCID 58293349 | — |
Reaction Steps
To a solution of an optically-active compound of [benzyl-(2-hydroxy-1-methylethyl)-amino]acetic acid tert-butyl ester (160.0 g) in chloroform (640 ml) cooled to 0° C. was added dropwise thionyl chloride (50.0 ml), and the mixture was stirred at 60° C. for 2 hours. The reaction mixture was cooled to 0° C. Then, thereto were added saturated aqueous sodium bicarbonate solution (1000 ml) and chloroform (100 ml), and the mixture was stirred. The separated organic layer was washed with saturated aqueous sodium chloride solution (500 ml), and the aqueous layer was extracted with chloroform (450 ml) again. The combined organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give the titled compound (172.9 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-4197bcef3b754de489e2486bb8ec9e1a |
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| Source note | uspto-grants-2013_12 |
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