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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1850046Generated: November 1, 2026

(Diethoxyphosphinyl)acetic acid → HCID 86702812, compound

https://huagongshe.com/reaction/1850046

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(Diethoxyphosphinyl)acetic acidHCID 36704—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-(tert-Butoxycarbonyl)-1,2-phenylenediamineHCID 676311—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
SolventDichloromethaneHCID 6344—
ProductHCID 86702812HCID 8670281276%

Reaction Steps

DIPEA (5.16 g, 6.90 mL, 40 mmol) and tert-butyl 2-aminophenylcarbamate (2.08 g, 10 mmol) were added to a solution of 2-(diethoxyphosphoryl)acetic acid (2.15 g, 11 mmol) in DCM (120 mL). After the mixture was stirred for ten minutes, HATU (4.56 g, 12 mmol) was added to the reaction and stirring was prolonged for 6 h at room temperature under a nitrogen atmosphere. After completion of the reaction as indicated by HPLC, the reaction mixture was washed with saturated NaHCO3 and brine. It was dried over Na2SO4 and filtered. The filtrate was evaporated in vacuo to get the crude product, which was triturated with 30% v/v hexanes in EtOAc for 30 min. The solid was filtered, washed with 30% hexanes in EtOAc and dried to get 2.92 g of tert-butyl (2-(2-(diethoxyphosphoryl)acetamido)phenyl)carbamate as an off-white solid in 76% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08957066B2
Source datasetuspto-grants-2015_02
ORD IDord-3b1657889f7d4530adc038e6f76beb18
Source noteuspto-grants-2015_02