HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1159441Generated: October 31, 2026
Isopropyl chloroformate → Isopropyl 4-Hydroxypiperidine-1-carboxylate
https://huagongshe.com/reaction/1159441
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropyl chloroformate | HCID 7917 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Solvent | Water | HCID 962 | — |
| Product | Isopropyl 4-Hydroxypiperidine-1-carboxylate | HCID 16745126 | 92% |
Reaction Steps
To a stirred mixture of 4-hydroxypiperidine (53.8 g, 1.000 eq), triethylamine (71.8 g, 1.334 equivalents), and ethyl acetate (498.8 g) was added neat isopropyl chloroformate (78.0 g, 1.1966 equivalents) at a rate sufficiently slow to maintain the reaction mixture temperature at 10°-17° C. with reactor jacket cooling. After the addition had been completed, the reaction mixture was stirred at 20° C. for 18 hours. Then water (100 g) was added, and the resulting mixture was stirred for 15 minutes before the phases were separated. The organic phase was washed with two 100-gram-portions of 20 wt % aqueous NaCl by stirring for 15 min at 150 rpm before separating the aqueous wash. After a final wash with water (100 g), the organic phase was concentrated by distillation on a rotary evaporator at reduced pressure to provide product (2) (91.1 g, 92.0% yield) as light amber oil of 96.8% purity by GC. Distillation of this crude product at 117-120° C., 0.3-1.0 torr gave a 95.7% recovery of product (2) as a colorless oil collected at 112°-119° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07812159B2 |
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| Source dataset | uspto-grants-2010_10 |
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| ORD ID | ord-af58ea6c39ae40359985fd41cea74561 |
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| Source note | uspto-grants-2010_10 |
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