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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 489875Generated: October 30, 2026

Ethanolamine → HCID 15929376, compound

https://huagongshe.com/reaction/489875

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-HydroxysuccinimideHCID 80170—
ReactantN-[tert-butoxycarbonyl]-L-serineHCID 98766—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
SolventDichloromethane methanolHCID 21226129—
SolventDCM MeOH AcOHHCID 21877243—
ProductHCID 15929376HCID 15929376—

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution comprising 6.15 g (30 mmol) of N-Boc-L-serine (1, Fluka) and 3.45 g of N-hydroxysuccinimide (30 mmol) in 80 ml of DMF is stirred at 0° C. and 6.2 g (30 mmol) of DCC are added. The reaction mixture is maintained at 0° C. for 15 min, then it is allowed to return to ambient temperature and stirring is continued for 1 h 30. 2.75 ml (60 mmol) of ethanolamine are subsequently added. After stirring for 12 h, the DCU formed is filtered off and washed with 2×15 ml of DMF. The combined organic phases are evaporated to dryness under vacuum. The product is isolated from the residual paste by flash chromatography on a silica gel column (Kieselgel Merck 60, 230-400 mesh; eluent: CH2Cl2/MeOH 6%). The expected compound is collected in the form of a gum which crystallizes from an AcOEt/hexane mixture to provide 5.21 g (Yd=70%) of colorless needles. Rf (CH2Cl2/MeOH, 9.3/0.7): 0.23; (CH2Cl2/MeOH/AcOH, 9/0.9/0.1): 0.47. M.p.=74-76° C. [α]D20=−2.2° (c 0.9, CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06979747B2
Source datasetuspto-grants-2005_12
ORD IDord-5d751103246f4f25a01771b7aa1b05ff
Source noteuspto-grants-2005_12