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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropyl chloroformateHCID 7917—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantPiperidin-4-olHCID 79341—
SolventWaterHCID 962—
ProductIsopropyl 4-Hydroxypiperidine-1-carboxylateHCID 1674512692%

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07812159B2
Source datasetuspto-grants-2010_10
ORD IDord-af58ea6c39ae40359985fd41cea74561
Source noteuspto-grants-2010_10