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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 363399Generated: October 29, 2026

1-Bromooctadecane → HCID 18705578, compound

https://huagongshe.com/reaction/363399

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BromooctadecaneHCID 8218—
ReactantEthyl 2-(diphenylmethyleneamino)acetateHCID 319508—
ReactantLithium HexamethyldisilazideHCID 2733832—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
Solvent2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl-HCID 81646—
ProductHCID 18705578HCID 1870557880%

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a stirred solution of N-(diphenylmethylene)-glycine ethyl ester (67.3 g, 0.250 mol) in a 1:1 mixture of anhydrous THF (500 ml) and DMPU (500 ml) at -78° C. under a dry argon atmosphere was added a solution of lithium bis(trimethylsilyl)amide (250 ml--1.0M in THF, 0.25 mol) over a 10 min period. The resulting orange solution was stirred for 1.5 h at -78° C. While maintaining the temperature at -78° C., a solution of 1-bromooctadecane (83.4 g, 0.250 mol) in a 1:1 mixture of anhydrous THF (250 ml) and DMPU (250 ml) was added over a 10 min period and the resulting mixture was allowed to warm to room temperature. After stirring the mixture for 17 h, H2O (50 ml) and then ethyl acetate (2 l) were added. The solution was washed with H2O (4×2 l). The solution was dried over Na2CO3 -Na2SO4 and the volume was reduced in vacuo to 1 l. The product was crystallized by the addition of hexane to give 104 g (80% yield) of an off-white crystalline solid: mp 62°-5° C.; 1H NMR (CDCl3) δ 0.88 (t, J =6.6 Hz, 3 H), 1.27 (m, 35 H), 1.90 (m, 2 H), 4.03 (m, 1 H), 4.17 (m, 2 H), 7.17 (m, 2 H), 7.36 (m, 6 H), 7.64 (m, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05874421
Source datasetuspto-grants-1999_02
ORD IDord-7eee34a9394347d88e933f3bac1dffc9
Source noteuspto-grants-1999_02