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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171289Generated: November 1, 2026

Triphosgene → 884504-55-6

https://huagongshe.com/reaction/2171289

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphosgeneHCID 94429—
ReactantTert-butyl 3-aminopropanoate hydrochlorideHCID 16218890—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product884504-55-6HCID 4472130793.8%

Reaction Steps

β-Alanine tert-butyl ester hydrochloride (13.0, 71.6 mmol) in CH2Cl2 (240 mL) and saturated NaHCO3(aq) solution (240 mL) was degassed and the flask was cooled in ice water bath. Triphosgene (21.2 g, 71.6 mmol) was added in one portion under inert atmosphere at 0° C. The reaction stirred at 0° C. to RT over 2.5 hr. The reaction was diluted with water (500 mL) and poured into reparatory funnel. The layers separated and the aqueous layer was extracted with CH2Cl2. The combined organic extracts were washed with brine, dried over Na2SO4, filtered, and concentrated under reduced pressure to obtain crude tert-butyl 3-iso cyanatopropionate (11.5 g) as a yellow liquid. This crude material was directly used for next reaction without purification. 1H NMR (300 MHz, CDCl3): δ 3.53 (t, 2H), 2.52 (t, 2H), 1.47 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051320B1
Source datasetuspto-grants-2015_06
ORD IDord-0ac10be906c64ba88036aa4c0c54150b
Source noteuspto-grants-2015_06