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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1450735Generated: October 25, 2026

Chloroform → 1-oxoheptyl-D-allo-Threonine

https://huagongshe.com/reaction/1450735

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroformHCID 6212—
ReactantSodium HydroxideHCID 14798—
ReactantHeptanoyl chlorideHCID 17313—
ReactantD-AllothreonineHCID 90624—
SolventTetrahydrofuranHCID 8028—
Product1-oxoheptyl-D-allo-ThreonineHCID 22851676—

Reaction Steps

A solution of n-heptanoyl chloride (440 mL, 2.83 mmol) in THF (250 mL) is added dropwise, over a period of 30 min, to a cold (-5° to 0° C.), vigorously stirred mixture of D-allo-Thr (300 mg, 2.51 mmol) and 2N aq. NaOH (3.5 mL, 7.0 meq) in THF (4.0 mL). The resulting mixture is stirred for 2 h at the same temperature and overnight at room temperature. The volatiles are removed and the residue is diluted with water and acidified, using conc. HCl. The mixture is extracted with EtOAc and the combined organic solution is washed with brine, dried, filtered, and concentrated to provide crude 2c-1 (420 mg, containing 10% excess heptanoyl reagent) which solidifies upon standing. NMR δ1.28 (d, J=6.5, 3 H), 4.20 (m, 1H), 4.61 (dd, J=3.4, 6.6, 1H), 6.56 (br d, J=6.9, 1H); [α]D26 -38±2 (CHCl3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05602275
Source datasetuspto-grants-1997_02
ORD IDord-4a049bcd42fa499e8f2fa5b49e702ff0
Source noteuspto-grants-1997_02