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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033779Generated: October 26, 2026

Sodium Hydroxide → HCID 178444544, compound

https://huagongshe.com/reaction/1033779

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% CH30H and 0.4% HOAc in CH2Cl2): NMR δ0.88 (t, J≃7, 3H), 4.15 (m, 1 H), 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 numberUS05312831
Source datasetuspto-grants-1994_05
ORD IDord-d8c3035e93d045239f92b7cb1929a63a
Source noteuspto-grants-1994_05