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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1087316Generated: October 31, 2026

Iodoethane → N-(tert-Butoxy(hydroxy)methylidene)-O-ethylserine

https://huagongshe.com/reaction/1087316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodoethaneHCID 6340—
ReactantN-[tert-butoxycarbonyl]-L-serineHCID 98766—
ReactantSodium MethoxideHCID 10942334—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductN-(tert-Butoxy(hydroxy)methylidene)-O-ethylserineHCID 15058451—

Reaction Steps

To a solution of 0.94 g BocSer in 66 mL THF was added a solution of 1.47 g NaOMe in 2.6 mL MeOH, followed by 11.7 g EtI. After 15 minutes, more NaOMe (0.49 g) and EtI (2 mL) were added and the reaction was stirred at RT overnight. More NaOMe and EtI were added and the reaction was stirred for an additional 6 hours. The mixture was concentrated in vacuo, dissolved in 25 mL H2O and washed 2×25 mL ether. The aqueous phase was acidified with concentrated HCl and extracted 4×25 mL CH2Cl2. The combined extracts were dried over MgSO4, filtered and concentrated in vacuo to 0.34 g crude product which carried on. NMR (300 MHz, CDCl3), delta 1.19 (t, J=7 Hz, 3H), 1.46 (s, 9H), 3.53 (q, J=7 Hz, 2H), 4.43 (m, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05034376
Source datasetuspto-grants-1991_07
ORD IDord-d412125b5fd74951b886bff242af0993
Source noteuspto-grants-1991_07