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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 52247Generated: October 24, 2026

Sodium Hydroxide → HCID 178444544, compound

https://huagongshe.com/en/reaction/52247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantOxalyl chlorideHCID 65578—
ReactantD-AllothreonineHCID 90624—
ReactantHCID 178444557HCID 178444557—
SolventTolueneHCID 1140—
SolventAcetonitrileHCID 6342—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178444544HCID 178444544—

Reaction Steps

A solution of trans-4-pentylcyclohexane carboxylic acid (198 mg, 1.0 mmol) in dry toluene (1 mL) is treated with oxalyl chloride (760 mg, 5.9 mmol) at 0° C. and the mixture is stirred for 2 h at the same temperature and 1 h at room temperature. Excess reagent is removed in vacuo. A solution of the crude acid chloride in dry acetonitrile (2 mL) is added to a mixture of D-allo-Thr (100 mg, 0.85 mmol), 2N aq. NaOH (600 μl, 1.20 meq) and TEA (85 mg, 0.85 mmol) in THF (1.5 mL), following the procedure described in Example 1. The crude product 2c-6 is purified by chromatography (1.5×18 cm column, 5% CH2OH and 0.4% HOAc in CH2Cl2): NMR δ0.88 (t, J-7, 3H), 4.15 (m, 1H), 4.54 (m, 1H), 6.49 (d, 1H); MS (CI, CH4) m/z 300 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05616612
Source datasetuspto-grants-1997_04
ORD IDord-fbd312348060406281a4d40b92aaf98a
Source noteuspto-grants-1997_04