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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1602047Generated: November 2, 2026

Phenylethanolamine → HCID 86754760, compound

https://huagongshe.com/reaction/1602047

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenylethanolamineHCID 1000—
ReactantTriethylamineHCID 8471—
ReactantAllyl chloroformateHCID 18052—
ReactantHCID 15247504HCID 15247504—
SolventDichloromethaneHCID 6344—
ProductHCID 86754760HCID 8675476092%

Reaction Steps

Synthesis of N-Allyloxycarbonyl-2-amino-1-phenylethanol (23) as illustrated in FIG. 5, reaction 4: ##STR12## Compound 23: Chemical method: 2-Amino-1-phenylethanol 15(0.50 g, 3.64 mmol) suspended in dry CH2Cl2 (20 mL) was treated with Et3N (triethylamine) (0.53 mL, 3.80 mmol) and allylchloroformate (0.41 mL, 3.86 mmol) for 30 min. The mixture was diluted with CH2Cl2 and washed with 1N KHSO4 and brine, dried (MgSO4), filtered and concentrated in vacuo. Silica gel column chromatography (eluent: CH2Cl2 /MeOH, 95/5, v/v) gave the desired product (742 mg) as a glass in 92% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05981267
Source datasetuspto-grants-1999_11
ORD IDord-1e8279fcb9c84bd3aa4c2de1bf027e08
Source noteuspto-grants-1999_11