HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098775Generated: October 25, 2026
Isopropanol → tert-Butyl ((1R,2S)-1-hydroxy-1-(3-methoxyphenyl)propan-2-yl)carbamate
https://huagongshe.com/reaction/1098775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Aluminum isopropoxide | HCID 11143 | — |
| Reactant | tert-Butyl [(1S)-2-(3-methoxyphenyl)-1-methyl-2-oxoethyl]carbamate | HCID 59339682 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-Butyl ((1R,2S)-1-hydroxy-1-(3-methoxyphenyl)propan-2-yl)carbamate | HCID 59339845 | 98.5% |
Reaction Steps
A mixture of tert-butyl [(1S)-2-(3-methoxyphenyl)-1-methyl-2-oxoethyl]carbamate (13.6 g, 48.7 mmol), aluminum isopropoxide (1.99 g, 9.70 mmol), 2-propanol (41 mL, 535 mmol) in toluene (63 mL) was stirred under an atmosphere of argon at 50° C. overnight. LC/MS showed complete conversion into the alcohol. The mixture was partitioned between ethyl acetate (200 mL) and hydrochloric acid (1M, 200 mL). The organic phase was washed with water (200 mL), dried over magnesium sulfate and concentrated to give the subtitle compound as a syrup (13.5 g). The compound was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08143290B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-2b43d01dd3054975bff97961cfaa410d |
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| Source note | uspto-grants-2012_03 |
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