Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421095Generated: October 31, 2026

Sodium hydride → HCID 15907745, compound

https://huagongshe.com/reaction/1421095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantMethyl GlycolateHCID 66774—
ReactantBenzene, 1-(chloromethyl)-3,5-dinitro-HCID 94673—
ReactantAcetone cardiceHCID 18522661—
SolventAcetic AcidHCID 176—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15907745HCID 1590774593%

Reaction Steps

To a solution of methyl glycolate (10 mL, 130 mmol) in THF (50 mL) at -70° C. (acetone-dry ice) was added in small portions, with stirring 60% NaH in oil (1.6 g, 111 mmol). To the resulting white suspension was added a solution of 3,5-dinitrobenzylchloride (5.0 g, 23 mmol). The reaction was allowed to warm to room temperature and acetic acid (2 mL) was added to quench excess NaH. The reaction mixture was concentrated and the residual tan oil was partitioned between water and CH2Cl2. The organic phase was washed with water and dried over Na2SO4. The crude product obtained after concentration was chromatographed on a silica gel column (4×25 cm) eluting with 33% ethyl acetate in hexane. Concentration of appropriate fractions followed by drying in vacuo gave 5.1 g (93%) of the desired product 2.1 as a pale yellow crystalline solid: 1H NMR (CDCl3) δ 8.98 (s, 1H, C4 --H), 8.59 (s, 2H, C2 --H), 4.85 (s, 2H, CH2), 4.29 (s, 2H, CH2), 3.81 (s, 3H, CH3); 13C NMR (CDCl3) δ 170.16, 148.58, 142.33, 127.30, 118.15, 71.10, 68.07, 52.18.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06072046
Source datasetuspto-grants-2000_06
ORD IDord-3166a6a1d3b74305b0a29a4edbe5e63a
Source noteuspto-grants-2000_06